Zinc Oxide
- Product NDC
- 64772-201
- 11-digit product format
- 647720201
- Labeler code
- 64772
- Product ID
- 64772-201_37eff762-1eaa-ec66-e063-6394a90a3d10
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide Ointment
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Derma Sciences Canada Inc.
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2014-11-03
- Substance
- ZINC OXIDE
- Active strength
- .2 g/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Zinc Oxide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | .2 g/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | SOI2LOH54Z |
| Rxcui | 198911 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 64772-201-01 | Zinc Oxide | 453.6 g in 1 JAR | OINTMENT | 453.6 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 64772-201-01 | 64772020101 | 453.6 g in 1 JAR (64772-201-01) | 453.6 g | 2014-11-03 | No | No | Historical |