Zinc Oxide 20%
- Product NDC
- 69396-086
- 11-digit product format
- 693960086
- Labeler code
- 69396
- Product ID
- 69396-086_0f4e022b-3f1e-96dc-e063-6294a90ad3b7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Trifecta Pharmaceuticals USA
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-05-30
- 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 20%
- 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 |
|---|
| 69396-086-02 | Zinc Oxide 20% | 60 g in 1 TUBE | OINTMENT | 60 | | 2 |
| 69396-086-02 | Zinc Oxide 20% | 1 in 1 BOX | OINTMENT | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69396-086 | ZINC OXIDE 20% (ZINC OXIDE) OINTMENT [TRIFECTA PHARMACEUTICALS USA] | 2 | Current NDC, 2 package rows | 20240120_fcef17f1-84e7-a288-e053-6294a90a064b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 69396-086-02 | 69396008602 | 1 TUBE in 1 BOX (69396-086-02) / 60 g in 1 TUBE | 1 tube | 2023-05-30 | No | No | Historical |