ULTRA SOOTHER DRY-TOUCH SUNSCREEN
- Product NDC
- 87534-150
- 11-digit product format
- 875340150
- Labeler code
- 87534
- Product ID
- 87534-150_4dbc1035-c41d-308c-e063-6394a90a36c4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- HOMOSALATE, OCTISALATE, OCTOCRYLENE, ZINC OXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- skinnplus
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-03-24
- Substance
- HOMOSALATE; OCTISALATE; OCTOCRYLENE; ZINC OXIDE
- Active strength
- 3; 2.25; 2.5; 5.19 g/50mL; g/50mL; g/50mL; g/50mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ULTRA SOOTHER DRY-TOUCH SUNSCREEN
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HOMOSALATE | 3 g/50mL |
| OCTISALATE | 2.25 g/50mL |
| OCTOCRYLENE | 2.5 g/50mL |
| ZINC OXIDE | 5.19 g/50mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | V06SV4M95S, 4X49Y0596W, 5A68WGF6WM, SOI2LOH54Z |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 87534-150-01 | ULTRA SOOTHER DRY-TOUCH SUNSCREEN | 50 mL in 1 TUBE | CREAM | 50 | | 1 |
| 87534-150-02 | ULTRA SOOTHER DRY-TOUCH SUNSCREEN | 1 in 1 BOX | CREAM | 1 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87534-150-01 | 87534015001 | 50 mL in 1 TUBE | 50 ml | | | | Historical |
| 87534-150-02 | 87534015002 | 1 TUBE in 1 BOX (87534-150-02) / 50 mL in 1 TUBE (87534-150-01) | 1 tube | 2026-03-24 | No | No | Historical |