Walgreens Sunburn Relief
- Product NDC
- 0363-0966
- 11-digit product format
- 003630966
- Labeler code
- 0363
- Product ID
- 0363-0966_24740d5a-aba3-0bd4-e063-6394a90ab2ca
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- WALGREEN COMPANY
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2017-09-11
- Substance
- MENTHOL
- Active strength
- 5 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Walgreens Sunburn Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 5 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 2564388 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0363-0966-15 | Walgreens Sunburn Relief | 170 g in 1 TUBE | GEL | 170 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0363-0966 | WALGREENS SUNBURN RELIEF (MENTHOL) GEL [WALGREEN COMPANY] | 2 | Current NDC, Legacy NDC, 1 package rows | 20241016_c8967fba-6c28-494b-e053-2995a90acbba.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0363-0966-15 | 00363096615 | 170 g in 1 TUBE (0363-0966-15) | 170 g | 2017-09-11 | 0000-00-00 | No | No | Current |