Astringent
- Product NDC
- 35192-005
- 11-digit product format
- 351920005
- Labeler code
- 35192
- Product ID
- 35192-005_6e2ff42f-edbc-4526-9f86-33cdb8c93d1e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aluminum Acetate
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- CA-BOTANA INTERNATIONAL
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2015-01-01
- Marketing end
- 0000-00-00
- Substance
- ALUMINUM ACETATE
- Active strength
- 0 mg/4mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 35192-005-04 | Astringent | 4 mL in 1 POUCH | GEL | 4 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 35192-005 | ASTRINGENT (ALUMINUM ACETATE) GEL [CA-BOTANA INTERNATIONAL] | 1 | Legacy NDC, 1 package rows | 20150211_912cbb41-de59-4062-9252-42b0a84f3aac.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 35192-005-04 | 35192000504 | 4 mL in 1 POUCH | 4 ml | Historical |