SKINSUIT FACE
- Product NDC
- 46007-204
- 11-digit product format
- 460070204
- Labeler code
- 46007
- Product ID
- 46007-204_2b39ef60-16c3-f252-e063-6394a90ae402
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ZINC OXIDE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Skin Authority LLC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2012-04-19
- Substance
- ZINC OXIDE
- Active strength
- 12 g/100mL
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- SKINSUIT FACE
- Brand name suffix
- SPF 50
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 12 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 |
|---|
| 46007-204-11 | SKINSUIT FACESPF 50 | 50 mL in 1 TUBE | LOTION | 50 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 46007-204 | SKINSUIT FACE SPF 50 (ZINC OXIDE) LOTION [SKIN AUTHORITY LLC] | 6 | Current NDC, Legacy NDC, 1 package rows | 20250110_389fc528-fda5-485a-ab37-f99fcf3ed0b3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 46007-204-11 | 46007020411 | 50 mL in 1 TUBE (46007-204-11) | 50 ml | 2020-01-02 | 0000-00-00 | No | No | Current |