Zinc oxide, Dimethicone
- Product NDC
- 79903-431
- 11-digit product format
- 799030431
- Labeler code
- 79903
- Product ID
- 79903-431_4e55f6fa-80c7-1a3b-e063-6394a90a5a16
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc oxide, Dimethicone
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Walmart Inc.
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-03-31
- Substance
- DIMETHICONE, UNSPECIFIED; ZINC OXIDE
- Active strength
- 200; 250 mg/mL; mg/mL
- Pharmacologic classes
- Skin Barrier Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Zinc oxide, Dimethicone
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DIMETHICONE, UNSPECIFIED | 200 mg/mL |
| ZINC OXIDE | 250 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 92RU3N3Y1O, SOI2LOH54Z |
| Rxcui | 968817 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 79903-431-01 | Zinc oxide, Dimethicone | 49 mL in 1 BOTTLE, SPRAY | SPRAY | 49 | | 4 |
| 79903-431-01 | Zinc oxide, Dimethicone | 1 in 1 CARTON | SPRAY | 1 | | 4 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 79903-431-01 | 79903043101 | 1 BOTTLE, SPRAY in 1 CARTON (79903-431-01) / 49 mL in 1 BOTTLE, SPRAY | 2026-03-31 | No | No | Current |