Sunburn Relief Gel
- Product NDC
- 72288-005
- 11-digit product format
- 722880005
- Labeler code
- 72288
- Product ID
- 72288-005_4c1f60dc-2a0b-ab72-e063-6394a90a5d4b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lidocaine HCl
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Amazon.com Services LLC
- 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 |
|---|
| 72288-005-34 | Sunburn Relief Gel | 226 g in 1 BOTTLE, PUMP | GEL | 226 | | 18 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72288-005 | SUNBURN RELIEF GEL (LIDOCAINE HCL) GEL [AMAZON.COM SERVICES LLC] | 16 | Current NDC, Legacy NDC, 1 package rows | 20240806_adb638ec-4a7c-42f2-b249-0ac53a8dd4b2.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 |
|---|
| 72288-005-34 | 72288000534 | 226 g in 1 BOTTLE, PUMP (72288-005-34) | 226 g | 2018-08-31 | 0000-00-00 | No | No | Current |