Dew Mineral
- Product NDC
- 87197-204
- 11-digit product format
- 871970204
- Labeler code
- 87197
- Product ID
- 87197-204_458a97ed-ac1c-1053-e063-6294a90a4c26
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- ADVANCED AESTHETIC DERMATOLOGY
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-11-01
- Substance
- ZINC OXIDE
- Active strength
- 200 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Dew Mineral
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 200 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | SOI2LOH54Z |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 87197-204-60 | Dew Mineral | 60 g in 1 BOTTLE, PUMP | CREAM | 60 | | 2 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87197-204-60 | 87197020460 | 60 g in 1 BOTTLE, PUMP (87197-204-60) | 60 g | 2023-11-01 | No | No | Historical |