Sunsovle MD Volumize and Restore
- Product NDC
- 84878-823
- 11-digit product format
- 848780823
- Labeler code
- 84878
- Product ID
- 84878-823_4395b9eb-a4d0-37e7-e063-6394a90aeaa2
- 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
- 2024-11-05
- Substance
- ZINC OXIDE
- Active strength
- 110 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
- Sunsovle MD Volumize and Restore
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 110 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 |
|---|
| 84878-823-01 | Sunsovle MD Volumize and Restore | 50 mL in 1 BOTTLE, DROPPER | LOTION | 50 | | 4 |
| 84878-823-02 | Sunsovle MD Volumize and Restore | 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 |
|---|
| 84878-823 | SUNSOVLE MD VOLUMIZE AND RESTORE (ZINC OXIDE) LOTION [SUNSOLVE MD INC] | 2 | Current NDC, 2 package rows | 20250507_26f3cdda-b990-15cb-e063-6394a90ade29.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84878-823-01 | 84878082301 | 50 mL in 1 BOTTLE, DROPPER | 50 ml | | | | Historical |
| 84878-823-02 | 84878082302 | 1 BOTTLE, DROPPER in 1 CARTON (84878-823-02) / 50 mL in 1 BOTTLE, DROPPER (84878-823-01) | | 2024-11-05 | No | No | Current |