Dabur India Ltd
FDA import alert and refusal historyBaddi, IndiaFEI 3007140482
As of October 26, 2026, Dabur India Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on March 30, 2026, most often for unapproved new drug (UNAPPROVED).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Holy basil (herbal & botanicals, not teas ii) · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Dabur India Ltd
3 records, newest first. Each line links to the FDA page it came from.
2026
- Import refusalRefused, Holy basil (herbal & botanicals, not teas ii)UNAPPROVEDEntry AEK-0113241-3Source
2017
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2016
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and EconSource
Refusal charges, in plain English
- UNAPPROVED1 refused line
Unapproved new drug
The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.
Questions about Dabur India Ltd
- Is Dabur India Ltd on an FDA import alert?
- No listing for Dabur India Ltd appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the India page.
- Has FDA refused shipments from Dabur India Ltd?
- Yes. FDA refused 1 shipment line from Dabur India Ltd on March 30, 2026. The most recent, on March 30, 2026, was holy basil (herbal & botanicals, not teas ii), charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Dabur India Ltd's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
- When was Dabur India Ltd last inspected by FDA?
- FDA's most recent inspection of Dabur India Ltd with a final classification is dated July 6, 2017 and was classified VAI (Voluntary Action Indicated).
- What is Dabur India Ltd's FEI number?
- Dabur India Ltd's FDA Establishment Identifier (FEI) is 3007140482.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.