Pain, Burn, and Itch Relief
- Product NDC
- 72839-343
- 11-digit product format
- 728390343
- Labeler code
- 72839
- Product ID
- 72839-343_29a5d04c-286a-9659-e063-6294a90a30bc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzocaine 20%, Menthol 0.5%
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Derma Care Research Labs, LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-01-30
- Substance
- BENZOCAINE; MENTHOL
- Active strength
- 20; .5 g/100g; g/100g
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], 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 |
|---|
| U3RSY48JW5 | BENZOCAINE | 94-09-7 | BENZOCAINE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72839-343-03 | 72839034303 | 85 g in 1 CAN (72839-343-03) | 85 g | 2023-01-30 | No | No | Historical |