SKINSUIT LIP
- Product NDC
- 46007-205
- 11-digit product format
- 460070205
- Labeler code
- 46007
- Product ID
- 46007-205_4642868b-77bd-411e-e063-6394a90ac676
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ZINC OXIDE
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Skin Authority LLC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-01-02
- Substance
- ZINC OXIDE
- Active strength
- 10 g/100g
- 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 LIP
- Brand name suffix
- SPF 30
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 10 g/100g |
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 |
|---|
| 46007-205-11 | SKINSUIT LIPSPF 30 | 3.2 g in 1 BOTTLE, WITH APPLICATOR | GEL | 3.2 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 46007-205 | SKINSUIT LIP SPF 30 (ZINC OXIDE) GEL [SKIN AUTHORITY LLC] | 6 | Current NDC, Legacy NDC, 1 package rows | 20250110_cb24d714-f6cd-4518-b146-627cfe6c2ccd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 46007-205-11 | 46007020511 | 3.2 g in 1 BOTTLE, WITH APPLICATOR (46007-205-11) | 3.2 g | 2020-01-02 | 0000-00-00 | No | No | Current |