Lantiseptic Dry Skin Therapy
- Product NDC
- 12090-0016
- 11-digit product format
- 120900016
- Labeler code
- 12090
- Product ID
- 12090-0016_451fa655-d1cb-4229-e054-00144ff88e88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- LANOLIN
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Santus LLC
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-03-02
- Marketing end
- 0000-00-00
- Substance
- LANOLIN
- Active strength
- 300 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record