NUDESCREEN DEWY ILLUMINATING GLOW SPF 30 - Sunkissed Glow
- Product NDC
- 54111-194
- 11-digit product format
- 541110194
- Labeler code
- 54111
- Product ID
- 54111-194_7a12c26c-723b-40cb-9960-8e7137c86d13
- 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
- 2026-03-23
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- NUDESCREEN DEWY ILLUMINATING GLOW SPF 30 - Sunkissed Glow
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 15 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 |
|---|
| 54111-194-01 | NUDESCREEN DEWY ILLUMINATING GLOW SPF 30 - Sunkissed Glow | 1 in 1 CARTON | LOTION | 1 | | 1 |
| 54111-194-01 | NUDESCREEN DEWY ILLUMINATING GLOW SPF 30 - Sunkissed Glow | 50 mL in 1 TUBE | LOTION | 50 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 54111-194-01 | 54111019401 | 1 TUBE in 1 CARTON (54111-194-01) / 50 mL in 1 TUBE | 1 tube | 2026-03-23 | No | No | Current |