Sunburn Relief Gel
- Product NDC
- 30400-605
- 11-digit product format
- 304000605
- Labeler code
- 30400
- Product ID
- 30400-605_2e7c3924-521f-00bc-e063-6294a90a35da
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lidocaine HCl
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Jell Pharmaceuticals Pvt. Ltd
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-02-19
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sunburn Relief Gel
- Listing expiration
- 2026-12-31
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 |
|---|
| 30400-605-01 | Sunburn Relief Gel | 170 g in 1 BOTTLE, PUMP | GEL | 170 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 30400-605 | SUNBURN RELIEF GEL (LIDOCAINE HCL) GEL [JELL PHARMACEUTICALS PVT. LTD] | 1 | Current NDC, 1 package rows | 20250308_2e7c49de-5438-4858-e063-6294a90ad98c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 30400-605-01 | 30400060501 | 170 g in 1 BOTTLE, PUMP (30400-605-01) | 170 g | 2025-02-19 | No | No | Historical |