Knesko Skin The Sunscreen
- Product NDC
- 87407-236
- 11-digit product format
- 874070236
- Labeler code
- 87407
- Product ID
- 87407-236_5114ef81-229c-690c-e063-6394a90a0cd0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Knesko, LLC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-04-20
- Substance
- ZINC OXIDE
- Active strength
- 132 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Knesko Skin The Sunscreen
- Listing expiration
- 2027-12-31
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 |
|---|
| 87407-236-01 | Knesko Skin The Sunscreen | 50 mL in 1 BOTTLE | LOTION | 50 | | 1 |
| 87407-236-02 | Knesko Skin The Sunscreen | 1 in 1 CARTON | LOTION | 1 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87407-236-01 | 87407023601 | 50 mL in 1 BOTTLE | 50 ml | | | | Historical |
| 87407-236-02 | 87407023602 | 1 BOTTLE in 1 CARTON (87407-236-02) / 50 mL in 1 BOTTLE (87407-236-01) | 1 bottle | 2026-04-20 | No | No | Current |