Pure Sunscreen
- Product NDC
- 79487-150
- 11-digit product format
- 794870150
- Labeler code
- 79487
- Product ID
- 79487-150_4eca5257-6844-2a33-e063-6394a90ade28
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Liz Corporation Ltd
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-04-06
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 1.5; 4; 2.25; 3 g/50g; g/50g; g/50g; g/50g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pure Sunscreen
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AVOBENZONE | 1.5 g/50g |
| HOMOSALATE | 4 g/50g |
| OCTISALATE | 2.25 g/50g |
| OCTOCRYLENE | 3 g/50g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | G63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 79487-150-01 | Pure Sunscreen | 50 g in 1 TUBE | CREAM | 50 | | 1 |
| 79487-150-02 | Pure 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 |
|---|
| 79487-150-01 | 79487015001 | 50 g in 1 TUBE | 50 g | | | | Historical |
| 79487-150-02 | 79487015002 | 1 TUBE in 1 BOX (79487-150-02) / 50 g in 1 TUBE (79487-150-01) | 1 tube | 2026-04-06 | No | No | Current |