Burn-B Gone OTC
- Product NDC
- 47341-002
- 11-digit product format
- 473410002
- Labeler code
- 47341
- Product ID
- 47341-002_a6b5ed46-bf0e-4e9e-8ced-a6645ee59148
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Burn-B Gone OTC
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Quantum Labs LLC
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2010-05-10
- Marketing end
- 0000-00-00
- Substance
- ALLANTOIN
- Active strength
- 1 g/75g
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 47341-002-20 | Burn-B Gone OTC | 75 g in 1 TUBE | GEL | 75 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 47341-002 | BURN-B GONE OTC GEL [QUANTUM LABS LLC] | 3 | Legacy NDC, 1 package rows | 20100519_ace3557b-a08f-4a6e-b911-0bc2fa42141a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 47341-002-20 | 47341000220 | 75 g in 1 TUBE | 75 g | Historical |