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Unique Fragrances

⚠️ High Risk

FEI: 3013257836 • New Delhi, Delhi • INDIA

FEI

FEI Number

3013257836

📍

Location

New Delhi, Delhi

🇮🇳

Country

INDIA
🏢

Address

1 Plot No 21, Road No, New Delhi, Delhi, India

High Risk

FDA Import Risk Assessment

61.3
LowModerateHighCritical

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

Statistics

14
Total Refusals
14
Unique Violations
2/20/2025
Latest Refusal
3/22/2016
Earliest Refusal

Score Breakdown

Violation Severity
75.6×40%
Refusal Volume
43.6×30%
Recency
82.2×20%
Frequency
15.7×10%
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

38789×

POISONORD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a poisonous or deleterious substance which would ordinarily render the article injurious to health. Contains:

2383×

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.

4822×

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.

1971×

COSM COLOR

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a color additive which is unsafe within the meaning of Section 721(a) which renders it adulterated under Section 601(e).

2181×

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.

2491×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

2561×

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)).

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.

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

3291×

JUICE %

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 the food purports to be a beverage containing vegetable or fruit juice and does not bear a statement on the label in appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained therein.

111×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

641×

YELLOW #5

The food appears to bear or contain the color additive FD & C Yellow No. 5, which is not declared on the label per 21 CFR 74.705(a)(c) under section 721.

1181×

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).

161×

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.

Refusal History

DateProductViolationsDivision
2/20/2025
33EGT13ROCK CANDY, HARD, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
3878POISONORD
Division of Northeast Imports (DNEI)
2/20/2025
33EGT13ROCK CANDY, HARD, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
3878POISONORD
Division of Northeast Imports (DNEI)
2/20/2025
33EGT13ROCK CANDY, HARD, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
3878POISONORD
Division of Northeast Imports (DNEI)
2/20/2025
33EGT13ROCK CANDY, HARD, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
3878POISONORD
Division of Northeast Imports (DNEI)
2/20/2025
28AGT40SAFFRON, WHOLE (SPICE)
3878POISONORD
Division of Northeast Imports (DNEI)
2/20/2025
33EGT13ROCK CANDY, HARD, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
3878POISONORD
Division of Northeast Imports (DNEI)
2/20/2025
23BGT14BETEL NUT, SHELLED
238UNSAFE ADD
3878POISONORD
Division of Northeast Imports (DNEI)
2/20/2025
23BGT14BETEL NUT, SHELLED
238UNSAFE ADD
3878POISONORD
Division of Northeast Imports (DNEI)
2/20/2025
23BGT14BETEL NUT, SHELLED
238UNSAFE ADD
3878POISONORD
Division of Northeast Imports (DNEI)
9/24/2019
53CK03EYE SHADOW (EYE MAKEUP PREPARATIONS)
197COSM COLOR
Division of West Coast Imports (DWCI)
9/4/2019
33EGT05CANDY BAR OR PIECES (NOT CARAMEL OR FONDANT), HARD, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
256INCONSPICU
64YELLOW #5
Division of West Coast Imports (DWCI)
8/1/2017
21VHY34AMLA, SUBTROPICAL AND TROPICAL FRUIT, JUICES, MILK, CREME, DRINKS AND NECTARS
218LIST INGRE
320LACKS FIRM
329JUICE %
482NUTRIT LBL
Division of West Coast Imports (DWCI)
8/25/2016
76EFTCLEANSER, DENTURE, OTC
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
San Francisco District Office (SAN-DO)
3/22/2016
23KGT06LOTUS SEED (EDIBLE SEED)
249FILTHY
482NUTRIT LBL
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Unique Fragrances's FDA import refusal history?

Unique Fragrances (FEI: 3013257836) has 14 FDA import refusal record(s) in our database, spanning from 3/22/2016 to 2/20/2025.

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. Unique Fragrances's FEI number is 3013257836.

What types of violations has Unique Fragrances received?

Unique Fragrances has been cited for 14 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 Unique Fragrances come from?

All FDA import refusal data for Unique Fragrances 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.