NUDESCREEN BLUSH TINT SPF 30- SUNSET ROSE
- Product NDC
- 54111-174
- 11-digit product format
- 541110174
- Labeler code
- 54111
- Product ID
- 54111-174_f2312c7b-13f8-4622-9c6e-a3104113a830
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ZINC OXIDE SUNSCREEN
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Bentley Laboratories, LLC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-12-27
- Substance
- ZINC OXIDE
- Active strength
- 15 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
- NUDESCREEN BLUSH TINT SPF 30- SUNSET ROSE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 15 g/100mL |
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 |
|---|
| 54111-174-01 | NUDESCREEN BLUSH TINT SPF 30- SUNSET ROSE | 1 in 1 CARTON | LOTION | 1 | | 3 |
| 54111-174-01 | NUDESCREEN BLUSH TINT SPF 30- SUNSET ROSE | 15 mL in 1 TUBE | LOTION | 15 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 54111-174 | NUDESCREEN BLUSH TINT SPF 30- SUNSET ROSE (ZINC OXIDE SUNSCREEN) LOTION [BENTLEY LABORATORIES, LLC] | 3 | Current NDC, 2 package rows | 20231230_e351dff2-4237-4458-a947-b894e7b670a3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 54111-174-01 | 54111017401 | 1 TUBE in 1 CARTON (54111-174-01) / 15 mL in 1 TUBE | 1 tube | 2023-12-27 | No | No | Current |