Sunburn Relief
- Product NDC
- 79903-037
- 11-digit product format
- 799030037
- Labeler code
- 79903
- Product ID
- 79903-037_eb2a46e0-74ec-4ed5-a383-d0a3a0fb73c7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lidocaine HCl 0.5%
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- WALMART INC.
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-12-23
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE HYDROCHLORIDE
- Active strength
- 1 g/100g
- Pharmacologic classes
- Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 79903-037 | SUNBURN RELIEF (LIDOCAINE HCL 0.5%) GEL [WALMART INC.] | 6 | Legacy NDC | 20241004_1eef58d3-7671-48f6-b4c4-4b83eae9d197.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 79903-037-34 | 79903003734 | 226 g in 1 BOTTLE, PLASTIC (79903-037-34) | 226 g | 2020-12-23 | 0000-00-00 | No | No | Current |