ZO MEDICAL SURFATROL Astringent
- Product NDC
- 42851-084
- 11-digit product format
- 428510084
- Labeler code
- 42851
- Product ID
- 42851-084_af2e1f39-b312-41f4-923c-18a4dff99e1f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aluminum Acetate
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- ZO Skin Health, Inc.
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-08-01
- Marketing end
- 0000-00-00
- Substance
- ALUMINUM ACETATE
- Active strength
- 4866 mg/4.866g
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#