NBE Anbesol
- Product NDC
- 0363-0316
- 11-digit product format
- 003630316
- Labeler code
- 0363
- Product ID
- 0363-0316_441e7c47-f347-a262-e063-6394a90ae697
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzocaine
- Dosage form
- GEL
- Route
- ORAL
- Labeler
- Walgreens
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-04-30
- Substance
- BENZOCAINE
- Active strength
- 20 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- NBE Anbesol
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZOCAINE | 20 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U3RSY48JW5 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0363-0316-69 | NBE Anbesol | 1 in 1 CARTON | GEL | 1 | | 6 |
| 0363-0316-69 | NBE Anbesol | 9 g in 1 TUBE | GEL | 9 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0363-0316 | NBE ANBESOL (BENZOCAINE) GEL [WALGREENS] | 4 | Current NDC, Legacy NDC, 2 package rows | 20250119_dd2a3125-32f8-5fff-e053-2995a90ac720.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0363-0316-69 | 00363031669 | 1 TUBE in 1 CARTON (0363-0316-69) / 9 g in 1 TUBE | 1 tube | 2022-06-22 | 0000-00-00 | No | No | Current |