ESIKA MEN 2 EN 1 ANTIDANDRUFF MULTI-ACTION
- Product NDC
- 13537-751
- 11-digit product format
- 135370751
- Labeler code
- 13537
- Product ID
- 13537-751_0500d778-7a1b-472b-8171-a6230814c9d6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Pyrithione Zinc
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Ventura Corporation LTD
- Application
- part358H
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2015-08-17
- Marketing end
- 0000-00-00
- Substance
- PYRITHIONE ZINC
- Active strength
- 0 g/mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#