Hasol Revitalizing Scalp Ampoule
- Product NDC
- 51270-116
- 11-digit product format
- 512700116
- Labeler code
- 51270
- Product ID
- 51270-116_cc5615fc-e259-4216-97ce-64454a5df4b8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALLANTOIN
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Ecomine Co Ltd
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2013-07-01
- Marketing end
- 0000-00-00
- Substance
- ALLANTOIN
- Active strength
- 0 g/10g
- 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 |
|---|
| 51270-116-01 | Hasol Revitalizing Scalp Ampoule | 10 g in 1 BOTTLE | LIQUID | 10 | | 1 |
| 51270-116-02 | Hasol Revitalizing Scalp Ampoule | 12 in 1 BOX | LIQUID | 12 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51270-116 | HASOL REVITALIZING SCALP AMPOULE (ALLANTOIN) LIQUID [ECOMINE CO LTD] | 1 | Legacy NDC, 2 package rows | 20130701_e3acf62d-4acd-4490-86df-c6e1d3c909ce.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 51270-116-01 | 51270011601 | 10 g in 1 BOTTLE | 10 g | Historical |
| 51270-116-02 | 51270011602 | 12 in 1 BOX | | Historical |