Ammonium Lactate
- Product NDC
- 72162-1413
- 11-digit product format
- 721621413
- Labeler code
- 72162
- Product ID
- 72162-1413_8c670756-f8c1-4bea-9eda-6b9e569debbe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ammonium Lactate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075774
- Marketing category
- ANDA
- Marketing start
- 2006-08-16
- Substance
- AMMONIUM LACTATE
- Active strength
- 12 g/100g
- Pharmacologic classes
- Acidifying Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 67M901L9NQ | AMMONIUM LACTATE | 515-98-0 | AMMONIUM LACTATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1413-2 | 72162141302 | 2 TUBE in 1 CARTON (72162-1413-2) / 140 g in 1 TUBE | 2 tube | 2023-08-16 | No | No | Historical |