ASCORBIC ACID
- Product NDC
- 43742-0561
- 11-digit product format
- 437420561
- Labeler code
- 43742
- Product ID
- 43742-0561_b11b2d5b-fc71-4d20-acaa-36a10dafc6aa
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ASCORBIC ACID
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-01-19
- Marketing end
- 2022-07-27
- Substance
- ASCORBIC ACID
- Active strength
- 6 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.
Dataset, Scope, Product NDC table| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|
| excluded product | product | 43742-0561 | | D | Discontinued by firm | | 2026-07-31 |
| excluded package | package | 43742-0561 | 43742-0561-1 | D | Discontinued by firm | | 2026-07-31 |
DailyMed Socrata Ingredients#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43742-0561-1 | 43742056101 | 30 mL in 1 BOTTLE, DROPPER (43742-0561-1) | 30 ml | 2015-01-19 | 2022-07-27 | No | No | Current |