FDA.reportPublic FDA data

DR. WALTONS

Product NDC
76271-001
11-digit product format
762710001
Labeler code
76271
Product ID
76271-001_c6e98d27-268e-4ab6-98d6-746b45d4c56c
Type
HUMAN OTC DRUG
Nonproprietary name
TALC
Dosage form
POWDER
Route
TOPICAL
Labeler
Dr. Waltons, Incorporated
Application
part347
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2011-07-09
Marketing end
0000-00-00
Substance
ALPHA-TOCOPHEROL; ZINC OXIDE
Active strength
5 g/675g; g/675g
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76271-001-022025-01-16C16284748780-197449f38-ce2d-f6ea-e053-dbdaa90aa7034c0dac58-34b5-418a-a54c-5ffcb690771f
76271-001-242025-01-16C16284748780-197449f38-ce2d-f6ea-e053-dbdaa90aa7034c0dac58-34b5-418a-a54c-5ffcb690771f
76271-001-022019-11-13C16284748780-197449f38-ce2d-f6ea-e053-dbdaa90aa7034c0dac58-34b5-418a-a54c-5ffcb690771f
76271-001-242019-11-13C16284748780-197449f38-ce2d-f6ea-e053-dbdaa90aa7034c0dac58-34b5-418a-a54c-5ffcb690771f