ORIGINAL POWER WHITENING AND LINELESS AMPOULE
- Product NDC
- 51346-219
- 11-digit product format
- 513460219
- Labeler code
- 51346
- Product ID
- 51346-219_cd6fd639-16ad-44d2-9d6c-754a2ae0d9d4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALLANTOIN
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- NATURE REPUBLIC CO., LTD.
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2013-02-01
- Marketing end
- 0000-00-00
- Substance
- ALLANTOIN
- Active strength
- 1 mg/30mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 51346-219-01 | ORIGINAL POWER WHITENING AND LINELESS AMPOULE | 30 mL in 1 CARTON | LIQUID | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51346-219 | ORIGINAL POWER WHITENING AND LINELESS AMPOULE (ALLANTOIN) LIQUID [NATURE REPUBLIC CO., LTD.] | 1 | Legacy NDC, 1 package rows | 20130530_8c72496d-ad42-4128-91df-3cf0cbbbde2d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 51346-219-01 | 51346021901 | 30 mL in 1 CARTON | 30 ml | Historical |