Mineral Sunscreen
- Product NDC
- 54111-183
- 11-digit product format
- 541110183
- Labeler code
- 54111
- Product ID
- 54111-183_8fbbcad3-e255-4f2a-9902-00f6316a253c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide Sunscreen
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Bentley Laboratories LLC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-12-15
- Substance
- ZINC OXIDE
- Active strength
- 12.025 g/100mL
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Mineral Sunscreen
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 12.025 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | SOI2LOH54Z |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 54111-183-01 | Mineral Sunscreen | 1 in 1 CARTON | CREAM | 1 | | 1 |
| 54111-183-01 | Mineral Sunscreen | 42 mL in 1 TUBE | CREAM | 42 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 54111-183 | MINERAL SUNSCREEN (ZINC OXIDE SUNSCREEN) CREAM [BENTLEY LABORATORIES LLC] | 1 | Current NDC, 2 package rows | 20241018_782a8641-7e6a-413b-a2ed-0efeb36c48a7.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 54111-183-01 | 54111018301 | 1 TUBE in 1 CARTON (54111-183-01) / 42 mL in 1 TUBE | 1 tube | 2020-12-15 | No | No | Current |