Ultra Whitening Ample
- Product NDC
- 70380-320
- 11-digit product format
- 703800320
- Labeler code
- 70380
- Product ID
- 70380-320_356500b9-605e-4272-bcae-116d0b581114
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Niacinamide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- MIGUHARA
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2016-01-02
- Marketing end
- 0000-00-00
- Substance
- NIACINAMIDE
- Active strength
- 1 g/35mL
- 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 |
|---|
| 70380-320-01 | Ultra Whitening Ample | 35 mL in 1 CARTON | CREAM | 35 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70380-320 | ULTRA WHITENING AMPLE (NIACINAMIDE) CREAM [MIGUHARA] | 1 | Legacy NDC, 1 package rows | 20160224_b057bfed-f530-487b-99e9-ca6e198e4480.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 70380-320-01 | 70380032001 | 35 mL in 1 CARTON | 35 ml | Historical |