Mineral Sun Drops
- Product NDC
- 69949-025
- 11-digit product format
- 699490025
- Labeler code
- 69949
- Product ID
- 69949-025_1461504e-866d-44d4-a4d9-60b2ba8ce33e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Synchronicity Spa, Inc. DBA Suntegrity
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-08-15
- Substance
- ZINC OXIDE
- Active strength
- 220 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
- Mineral Sun Drops
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 220 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 |
|---|
| 69949-025-01 | Mineral Sun Drops | 30 mL in 1 BOTTLE, DROPPER | LOTION | 30 | | 1 |
| 69949-025-01 | Mineral Sun Drops | 1 in 1 BOX | LOTION | 1 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 69949-025-01 | 69949002501 | 1 BOTTLE, DROPPER in 1 BOX (69949-025-01) / 30 mL in 1 BOTTLE, DROPPER | 2025-08-15 | No | No | Current |