LavaDerm AfterSun
- Product NDC
- 70631-067
- 11-digit product format
- 706310067
- Labeler code
- 70631
- Product ID
- 70631-067_4f8770bb-310d-48d9-e063-6294a90afcdb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Young Living Essential Oils, LC.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-04-18
- Substance
- MENTHOL
- Active strength
- .5 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- LavaDerm AfterSun
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | .5 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 1314935 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70631-067-57 | LavaDerm AfterSun | 1 in 1 BOX | SPRAY | 1 | | 4 |
| 70631-067-57 | LavaDerm AfterSun | 57 g in 1 BOTTLE, SPRAY | SPRAY | 57 | | 4 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70631-067-57 | 70631006757 | 1 BOTTLE, SPRAY in 1 BOX (70631-067-57) / 57 g in 1 BOTTLE, SPRAY | 2024-04-18 | No | No | Current |