Hindustan Unilever Ltd.
FDA import alert and refusal historyMumbai, IndiaFEI 13599
As of October 26, 2026, Hindustan Unilever Ltd. (Mumbai, India) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for custard powder vanilla brown and polson; custard powder; kissan mixed fruit jam; mixed fruit jam "fruit kick", published by FDA on October 2, 2009, is also listed on Import Alert 99-21 (red list), and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 45-02 · red listIA 99-21 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Hindustan Unilever Ltd.
2 records, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-21red listMixed Fruit JamSource
- Import alert listingListed on Import Alert 45-02red listCustard Powder Vanilla Brown and Polson; Custard Powder; Kissan Mixed Fruit Jam; Mixed Fruit Jam "Fruit Kick"Source
Questions about Hindustan Unilever Ltd.
- Is Hindustan Unilever Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, Hindustan Unilever Ltd. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for custard powder vanilla brown and polson; custard powder; kissan mixed fruit jam; mixed fruit jam "fruit kick"; FDA published the listing on October 2, 2009.
- Has FDA refused shipments from Hindustan Unilever Ltd.?
- No FDA import refusals for Hindustan Unilever Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Hindustan Unilever Ltd.'s FEI number?
- Hindustan Unilever Ltd.'s FDA Establishment Identifier (FEI) is 13599.
- Can shipments from Hindustan Unilever Ltd. still enter the U.S.?
- Shipments of custard powder vanilla brown and polson; custard powder; kissan mixed fruit jam; mixed fruit jam "fruit kick" from Hindustan Unilever Ltd. can be detained without physical examination under Import Alert 45-02; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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