PINK BEACH SUNSCREEN BODY BROAD SPECTRUM SPF 50
- Product NDC
- 82800-030
- 11-digit product format
- 828000030
- Labeler code
- 82800
- Product ID
- 82800-030_4874e605-65ff-fc3e-e063-6394a90a7146
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sunscreen
- Dosage form
- OIL
- Route
- TOPICAL
- Labeler
- The Center Brands, LLC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-01-25
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 3; 10; 5; 10 mg/100mg; mg/100mg; mg/100mg; mg/100mg
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- PINK BEACH SUNSCREEN BODY BROAD SPECTRUM SPF 50
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AVOBENZONE | 3 mg/100mg |
| HOMOSALATE | 10 mg/100mg |
| OCTISALATE | 5 mg/100mg |
| OCTOCRYLENE | 10 mg/100mg |
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 |
|---|
| 82800-030-01 | PINK BEACH SUNSCREEN BODY BROAD SPECTRUM SPF 50 | 1 in 1 PACKAGE | OIL | 1 | | 7 |
| 82800-030-01 | PINK BEACH SUNSCREEN BODY BROAD SPECTRUM SPF 50 | 118 mg in 1 TUBE | OIL | 118 | | 7 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82800-030-01 | 82800003001 | 1 TUBE in 1 PACKAGE (82800-030-01) / 118 mg in 1 TUBE | 1 tube | 2024-01-25 | No | No | Current |