Scarderm
- Product NDC
- 55264-050
- 11-digit product format
- 552640050
- Labeler code
- 55264
- Product ID
- 55264-050_1898cb5a-7a8a-41f4-8864-d9a7f262677a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Allantoin
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Sinsin Pharmaceutical Co., Ltd.
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-05-30
- Marketing end
- 0000-00-00
- Substance
- ALLANTOIN
- Active strength
- 10 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 55264-050-01 | Scarderm | 20 g in 1 TUBE | GEL | 20 | | 1 |
| 55264-050-01 | Scarderm | 1 in 1 BOX | GEL | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55264-050 | SCARDERM (ALLANTOIN) GEL [SINSIN PHARMACEUTICAL CO., LTD.] | 1 | Legacy NDC, 2 package rows | 20160606_f2ce685d-4a58-4a89-83fd-ceb3cb185325.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55264-050-01 | 55264005001 | 1 TUBE in 1 BOX (55264-050-01) > 20 g in 1 TUBE | 1 tube | 2016-05-30 | 0000-00-00 | No | No | Current |