Sunburn Relief Gel
- Product NDC
- 69842-909
- 11-digit product format
- 698420909
- Labeler code
- 69842
- Product ID
- 69842-909_4eccc1a9-c401-8866-e063-6394a90a118e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lidocaine HCl
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- CVS Pharmacy, Inc.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-08-31
- Substance
- LIDOCAINE HYDROCHLORIDE
- Active strength
- 5 mg/g
- Pharmacologic classes
- Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sunburn Relief Gel
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LIDOCAINE HYDROCHLORIDE | 5 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | V13007Z41A |
| Rxcui | 1011849 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69842-909-34 | Sunburn Relief Gel | 226 g in 1 BOTTLE, PUMP | GEL | 226 | | 15 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69842-909 | SUNBURN RELIEF GEL (LIDOCAINE HCL) GEL [CVS] | 12 | Current NDC, Legacy NDC, 1 package rows | 20241027_d7f52394-5cc1-48a6-ae89-9fc63b515758.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 |
|---|
| 69842-909-34 | 69842090934 | 226 g in 1 BOTTLE, PUMP (69842-909-34) | 226 g | 2018-08-31 | 0000-00-00 | No | No | Current |