Salicylic acid foot gel
- Product NDC
- 84025-321
- 11-digit product format
- 840250321
- Labeler code
- 84025
- Product ID
- 84025-321_2b3d5a13-b933-8887-e063-6294a90a3f61
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Salicylic acid foot gel
- Dosage form
- GEL
- Route
- CUTANEOUS
- Labeler
- Guangzhou Yanxi Biotechnology Co., Ltd
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-01-09
- Substance
- GLYCERIN; MINERAL OIL
- Active strength
- 3; 5 mg/100mL; mg/100mL
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Glycerol [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Chemical Allergen [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| PDC6A3C0OX | GLYCERIN | 56-81-5 | GLYCERIN |
| T5L8T28FGP | MINERAL OIL | 8042-47-5 | MINERAL OIL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84025-321-01 | 84025032101 | 100 mL in 1 BOTTLE (84025-321-01) | 100 ml | 2025-01-09 | No | No | Historical |