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Dabur India Limited, Sahibabad Unit

⚠️ High Risk

FEI: 3004326829 • Ghaziabad, Uttar Pradesh • INDIA

FEI

FEI Number

3004326829

📍

Location

Ghaziabad, Uttar Pradesh

🇮🇳

Country

INDIA
🏢

Address

Plot No. 22, Site IV, Sahibabad, Ghaziabad, Uttar Pradesh, India

High Risk

FDA Import Risk Assessment

62.4
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

44
Total Refusals
20
Unique Violations
4/6/2025
Latest Refusal
6/25/2003
Earliest Refusal

Score Breakdown

Violation Severity
62.7×40%
Refusal Volume
61.2×30%
Recency
84.5×20%
Frequency
20.2×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

7523×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

11810×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

4828×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

3245×

NO ENGLISH

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

165×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

2384×

UNSAFE ADD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.

2183×

LIST INGRE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

3212×

LACKS N/C

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

2562×

INCONSPICU

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

3282×

USUAL NAME

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

29202×

PESTICIDES

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:

3311×

DR QUALITC

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the drug appears to be represented as not being recognized in an official compendium and appears its strength differs from or its quality or purity falls below, that which it purports or is represented to possess.

3351×

LACKS N/C

The article is in package form and appears to not have a label containing an accurate statement of the quantity of the contents in terms of weight, measure or numerical count and no variations or exemptions have been prescribed by regs.

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

4751×

COSMETLBLG

It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.

4881×

HEALTH C

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling bears an unauthorized nutrient content/health claim.

23001×

DIETARYLBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.

3201×

LACKS FIRM

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

2601×

FALSE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

3301×

UNSAFE COL

The article appears to be a color additive for the purposes of coloring only in or on drugs or devices, and is unsafe within the meaning of Section 721(a).

Refusal History

DateProductViolationsDivision
4/6/2025
66VDA99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
4/6/2025
66VDA99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/22/2024
66VBR99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
Division of Northeast Imports (DNEI)
10/15/2021
54FGY99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/17/2020
66CAY99STOOL SOFTENER N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
10/8/2020
66VIA99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)
10/8/2020
54FBR99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
9/4/2019
28YGY99SPICES, FLAVORS AND SALT NOT MENTIONED ELSEWHERE, N.E.C.
324NO ENGLISH
328USUAL NAME
Division of Southeast Imports (DSEI)
9/4/2019
28YGY99SPICES, FLAVORS AND SALT NOT MENTIONED ELSEWHERE, N.E.C.
324NO ENGLISH
328USUAL NAME
Division of Southeast Imports (DSEI)
6/16/2016
66VCS99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
Division of Northeast Imports (DNEI)
8/5/2014
53IC01DENTIFRICES (AEROSOL, LIQUID, TOOTHPASTES, TOOTHPOWDERS), WITHOUT FLUORIDE (ORAL HYGIENE PRODUCTS)
473LABELING
Southwest Import District Office (SWI-DO)
5/23/2014
63RBJ06STANNOUS FLUORIDE (DENTAL CARIES PROPHYLACTIC)
118NOT LISTED
16DIRECTIONS
330UNSAFE COL
New York District Office (NYK-DO)
3/20/2014
54FCY99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
75UNAPPROVED
Los Angeles District Office (LOS-DO)
3/20/2014
54FCY99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
75UNAPPROVED
Los Angeles District Office (LOS-DO)
3/20/2014
54FCY99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
75UNAPPROVED
Los Angeles District Office (LOS-DO)
11/6/2013
66YBA99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
75UNAPPROVED
Los Angeles District Office (LOS-DO)
11/6/2013
66YBL99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
75UNAPPROVED
Los Angeles District Office (LOS-DO)
9/24/2012
26CD11MUSTARD OIL, REFINED, SINGLE INGREDIENT, SEE 28O FOR MUSTARD OIL AS A FLAVORING
238UNSAFE ADD
San Francisco District Office (SAN-DO)
9/24/2012
26CD11MUSTARD OIL, REFINED, SINGLE INGREDIENT, SEE 28O FOR MUSTARD OIL AS A FLAVORING
238UNSAFE ADD
San Francisco District Office (SAN-DO)
8/14/2012
66VBL99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
Chicago District Office (CHI-DO)
8/14/2012
66VBY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
Chicago District Office (CHI-DO)
3/15/2012
54FYE99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
256INCONSPICU
324NO ENGLISH
482NUTRIT LBL
San Francisco District Office (SAN-DO)
3/15/2012
54FYE99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
256INCONSPICU
324NO ENGLISH
482NUTRIT LBL
San Francisco District Office (SAN-DO)
3/15/2012
66V99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
16DIRECTIONS
75UNAPPROVED
San Francisco District Office (SAN-DO)
12/27/2011
62ICA85LETROZOLE (ANTI-NEOPLASTIC)
75UNAPPROVED
New Orleans District Office (NOL-DO)
10/27/2011
54FYY99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
2920PESTICIDES
New York District Office (NYK-DO)
9/19/2011
66VCS99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
New York District Office (NYK-DO)
5/17/2011
66YBY99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
118NOT LISTED
16DIRECTIONS
75UNAPPROVED
New York District Office (NYK-DO)
4/4/2011
54FYY99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
238UNSAFE ADD
Chicago District Office (CHI-DO)
1/5/2011
63BDH99BRONCHODILATOR N.E.C.
118NOT LISTED
75UNAPPROVED
New York District Office (NYK-DO)
5/12/2009
66VBY99MISCELLANEOUS PATENT MEDICINES, ETC.
16DIRECTIONS
75UNAPPROVED
Southwest Import District Office (SWI-DO)
5/12/2009
66VBY99MISCELLANEOUS PATENT MEDICINES, ETC.
16DIRECTIONS
75UNAPPROVED
Southwest Import District Office (SWI-DO)
5/6/2009
54EBH99HERBALS & BOTANICAL TEAS, N.E.C.
2920PESTICIDES
New York District Office (NYK-DO)
5/19/2008
33EGT12MIXED/ASSORTED HARD CANDY WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
321LACKS N/C
482NUTRIT LBL
San Francisco District Office (SAN-DO)
5/19/2008
33EGT12MIXED/ASSORTED HARD CANDY WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
218LIST INGRE
260FALSE
324NO ENGLISH
482NUTRIT LBL
San Francisco District Office (SAN-DO)
4/10/2007
54FCC99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
218LIST INGRE
San Francisco District Office (SAN-DO)
2/7/2007
33YGY99CANDY WITHOUT CHOCOLATE N.E.C.
218LIST INGRE
320LACKS FIRM
482NUTRIT LBL
Southwest Import District Office (SWI-DO)
10/6/2006
45LC99FLAVORING AGENTS AND ADJUVANTS (FOOD ADDITIVES FOR HUMAN USE)
75UNAPPROVED
San Francisco District Office (SAN-DO)
8/23/2006
53IG01DENTIFRICES (AEROSOL, LIQUID, TOOTHPASTES, TOOTHPOWDERS), WITHOUT FLUORIDE (ORAL HYGIENE PRODUCTS)
475COSMETLBLG
San Francisco District Office (SAN-DO)
3/30/2005
66VAR99MISCELLANEOUS PATENT MEDICINES, ETC.
331DR QUALITC
335LACKS N/C
New Orleans District Office (NOL-DO)
11/5/2004
54FER99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
2300DIETARYLBL
321LACKS N/C
482NUTRIT LBL
488HEALTH C
Atlanta District Office (ATL-DO)
1/8/2004
54YBR99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
482NUTRIT LBL
Seattle District Office (SEA-DO)
8/1/2003
26CGT11MUSTARD OIL, REFINED, SINGLE INGREDIENT, SEE 28O FOR MUSTARD OIL AS A FLAVORING
238UNSAFE ADD
482NUTRIT LBL
Seattle District Office (SEA-DO)
6/25/2003
53ED07TONICS, DRESSINGS, AND OTHER HAIR GROOMING AIDS (HAIR PREPARATIONS, NON-COLORING)
75UNAPPROVED
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Dabur India Limited, Sahibabad Unit's FDA import refusal history?

Dabur India Limited, Sahibabad Unit (FEI: 3004326829) has 44 FDA import refusal record(s) in our database, spanning from 6/25/2003 to 4/6/2025.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Dabur India Limited, Sahibabad Unit's FEI number is 3004326829.

What types of violations has Dabur India Limited, Sahibabad Unit received?

Dabur India Limited, Sahibabad Unit has been cited for 20 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about Dabur India Limited, Sahibabad Unit come from?

All FDA import refusal data for Dabur India Limited, Sahibabad Unit is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.