zinc oxide
- Product NDC
- 58029-223
- 11-digit product format
- 580290223
- Labeler code
- 58029
- Product ID
- 58029-223_8dc6340b-dc85-499c-bc87-a188e1629133
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- zinc oxide
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Gerimedix Incorporated
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2011-02-01
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 2 g/100g
- 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 |
|---|
| 58029-223-02 | zinc oxide | 24 in 1 CASE | OINTMENT | 24 | | 7 |
| 58029-223-02 | zinc oxide | 114 g in 1 TUBE | OINTMENT | 114 | | 7 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58029-223 | ZINC OXIDE OINTMENT [GERIMEDIX INCORPORATED] | 7 | Legacy NDC, 2 package rows | 20140904_d3b983d5-535e-4cd1-92ce-dcefd78ab192.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 58029-223-02 | 58029022302 | 24 in 1 CASE | Historical |