Dermadrox
- Product NDC
- 54162-220
- 11-digit product format
- 541620220
- Labeler code
- 54162
- Product ID
- 54162-220_f4238cc8-536d-4900-ae6e-ddb3b3cc9fbb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Acetate
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Geritrex LLC
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2015-07-31
- Marketing end
- 0000-00-00
- Substance
- ZINC ACETATE
- Active strength
- 1 g/118mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 54162-220-14 | Dermadrox | 118 mL in 1 BOTTLE, SPRAY | SPRAY | 118 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 54162-220 | DERMADROX (ZINC ACETATE) SPRAY [GERITREX LLC] | 1 | Legacy NDC, 1 package rows | 20160504_87dc161d-aaef-4ff3-8d26-a301ea9cd6c5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 54162-220-14 | 54162022014 | 118 mL in 1 BOTTLE, SPRAY | 118 ml | Historical |