ZINC OXIDE
- Product NDC
- 11822-0081
- 11-digit product format
- 118220081
- Labeler code
- 11822
- Product ID
- 11822-0081_0a9bbc5a-bc61-439e-b7ea-35247478e10c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ZINC OXIDE
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- RiteAid
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2009-05-19
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 200 mg/g
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 11822-0081-3 | ZINC OXIDE | 57 g in 1 TUBE | OINTMENT | 57 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-0081 | ZINC OXIDE OINTMENT [RITEAID] | 2 | Legacy NDC, 1 package rows | 20110720_8a3421c6-8533-4e93-b31d-f497fe33c80b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 11822-0081-3 | 11822008103 | 57 g in 1 TUBE | 57 g | Historical |