Poolside Butter Screen SPF 30 Sunscreen Butter
- Product NDC
- 85179-015
- 11-digit product format
- 851790015
- Labeler code
- 85179
- Product ID
- 85179-015_47a85fcf-2f0b-6a0d-e063-6394a90a3bd4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- I World LLC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-12-17
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 30; 150; 50; 100 mg/g; mg/g; mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Poolside Butter Screen SPF 30 Sunscreen Butter
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AVOBENZONE | 30 mg/g |
| HOMOSALATE | 150 mg/g |
| OCTISALATE | 50 mg/g |
| OCTOCRYLENE | 100 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | G63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85179-015-00 | Poolside Butter Screen SPF 30 Sunscreen Butter | 80 g in 1 BOTTLE | LIQUID | 80 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85179-015-00 | 85179001500 | 80 g in 1 BOTTLE (85179-015-00) | 80 g | 2025-12-17 | No | No | Current |