Sunsolve MD Correct and Fade
- Product NDC
- 84878-200
- 11-digit product format
- 848780200
- Labeler code
- 84878
- Product ID
- 84878-200_4395a3a6-6fe6-e6b9-e063-6294a90ae938
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Sunsolve MD Inc
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-11-06
- 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
- Sunsolve MD Correct and Fade
- 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 |
|---|
| 84878-200-01 | Sunsolve MD Correct and Fade | 48 mL in 1 BOTTLE, PUMP | LOTION | 48 | | 4 |
| 84878-200-02 | Sunsolve MD Correct and Fade | 1 in 1 CARTON | LOTION | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 84878-200 | SUNSOLVE MD CORRECT AND FADE (ZINC OXIDE) LOTION [SUNSOLVE MD INC] | 2 | Current NDC, 2 package rows | 20250507_26f3ad9f-f8ca-05d4-e063-6394a90ad5c4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84878-200-01 | 84878020001 | 48 mL in 1 BOTTLE, PUMP | 48 ml | | | | Historical |
| 84878-200-02 | 84878020002 | 1 BOTTLE, PUMP in 1 CARTON (84878-200-02) / 48 mL in 1 BOTTLE, PUMP (84878-200-01) | | 2024-11-06 | No | No | Current |