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Product NDC
51346-038
11-digit product format
513460038
Labeler code
51346
Product ID
51346-038_bf682ead-4d76-4489-bc50-f28212a16d84
Type
HUMAN OTC DRUG
Nonproprietary name
OCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE
Dosage form
CREAM
Route
TOPICAL
Labeler
NATURE REPUBLIC CO., LTD.
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2012-01-02
Marketing end
0000-00-00
Substance
OCTINOXATE; OCTISALATE; ZINC OXIDE; TITANIUM DIOXIDE
Active strength
4 g/50mL; g/50mL; g/50mL; g/50mL
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-038-012021-06-29C16284748780-19d75b9d0-4948-f424-e053-dadaa90a57ce02b9558d-53ac-4f05-aafa-045a04ad82a1
51346-038-012020-01-31C16284748780-19d75b9d0-4948-f424-e053-dadaa90a57ce02b9558d-53ac-4f05-aafa-045a04ad82a1