burnrelief
- Product NDC
- 56062-942
- 11-digit product format
- 560620942
- Labeler code
- 56062
- Product ID
- 56062-942_4a1a3ba7-17ef-6d13-e063-6294a90af950
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lidocaine HCl
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Publix Super Markets, Inc.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2017-01-10
- 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
- burnrelief
- 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 |
|---|
| 56062-942-34 | burnrelief | 226 g in 1 BOTTLE, PUMP | GEL | 226 | | 17 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 56062-942 | BURNRELIEF (LIDOCAINE HCL) GEL [PUBLIX] | 15 | Current NDC, Legacy NDC, 1 package rows | 20241024_9660f5e1-d39e-4f86-bf96-dff0f3bb729d.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 |
|---|
| 56062-942-34 | 56062094234 | 226 g in 1 BOTTLE, PUMP (56062-942-34) | 226 g | 2017-01-10 | 0000-00-00 | No | No | Current |