ESIKA
- Product NDC
- 13537-142
- 11-digit product format
- 135370142
- Labeler code
- 13537
- Product ID
- 13537-142_95ec8aef-349a-4a80-9d00-704219f1d175
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aluminum Sesquichlorohydrate
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Ventura Corporation Ltd.
- Application
- part350
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2011-12-13
- Marketing end
- 0000-00-00
- Substance
- ALUMINUM SESQUICHLOROHYDRATE
- 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#