Walgreens Sunburn Relief
- Product NDC
- 0363-0985
- 11-digit product format
- 003630985
- Labeler code
- 0363
- Product ID
- 0363-0985_247454aa-fa4d-51ef-e063-6394a90ab958
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lidocaine
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- WALGREEN COMPANY
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2017-10-03
- Substance
- LIDOCAINE
- Active strength
- 8 mg/g
- Pharmacologic classes
- Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
- 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 |
|---|
| LIDOCAINE | 8 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 98PI200987 |
| Rxcui | 1098616 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0363-0985-68 | Walgreens Sunburn Relief | 453 g in 1 BOTTLE | GEL | 453 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0363-0985 | WALGREENS SUNBURN RELIEF (LIDOCAINE) GEL [WALGREEN COMPANY] | 3 | Current NDC, Legacy NDC, 1 package rows | 20241016_d5067903-c559-dc6d-e053-2995a90a8ee3.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 |
|---|
| 0363-0985-68 | 00363098568 | 453 g in 1 BOTTLE (0363-0985-68) | 453 g | 2017-11-08 | 0000-00-00 | No | No | Current |