GD11 Rx SCM C5
- Product NDC
- 62171-100
- 11-digit product format
- 621710100
- Labeler code
- 62171
- Product ID
- 62171-100_bbc9fd79-64bd-4764-b770-eb6451853a2f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MANNITOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Coson Co., Ltd.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2017-07-01
- Marketing end
- 0000-00-00
- Substance
- MANNITOL
- Active strength
- 0 g/2mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 | 62171-100 | | D | Discontinued by firm | | 2026-07-31 |
| excluded package | package | 62171-100 | 62171-100-02 | D | Discontinued by firm | | 2026-07-31 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62171-100 | GD11 RX SCM C5 (MANNITOL) LIQUID [COSON CO., LTD.] | 1 | Legacy NDC | 20170824_64654bc7-b829-430b-a382-eb776f5f0edb.zip |