Solarium Daily Essentials Luminizing Glow Drops
- Product NDC
- 84891-2191
- 11-digit product format
- 848912191
- Labeler code
- 84891
- Product ID
- 84891-2191_43cc8ed8-24ef-87bb-e063-6394a90a5f8f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Solarium Brands LLC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-12-20
- Substance
- ZINC OXIDE
- Active strength
- 132 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Solarium Daily Essentials Luminizing Glow Drops
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 132 mg/mL |
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 |
|---|
| 84891-2191-1 | Solarium Daily Essentials Luminizing Glow Drops | 30 mL in 1 TUBE | LOTION | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 84891-2191 | SOLARIUM DAILY ESSENTIALS LUMINIZING GLOW DROPS (ZINC OXIDE) LOTION [SOLARIUM BRANDS LLC] | 1 | Current NDC, 1 package rows | 20250315_302a4efe-d429-b1c4-e063-6294a90a073d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84891-2191-1 | 84891219101 | 30 mL in 1 TUBE (84891-2191-1) | 30 ml | 2024-12-20 | No | No | Current |