Mulberry Emulsion
- Product NDC
- 69969-005
- 11-digit product format
- 699690005
- Labeler code
- 69969
- Product ID
- 69969-005_7375e21c-85cf-4466-a6ad-20468306d403
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALLANTOIN
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- CORPORATION SORISO
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2015-07-10
- Marketing end
- 0000-00-00
- Substance
- ALLANTOIN
- Active strength
- 0 g/100mL
- 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 |
|---|
| 69969-005-01 | Mulberry Emulsion | 130 mL in 1 BOTTLE | LIQUID | 130 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69969-005 | MULBERRY EMULSION (ALLANTOIN) LIQUID [CORPORATION SORISO] | 1 | Legacy NDC, 1 package rows | 20150711_a98973e7-850c-441f-8b1d-71f9fed59c45.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 69969-005-01 | 69969000501 | 130 mL in 1 BOTTLE | 130 ml | Historical |