SUNSCREEN GLOWING
- Product NDC
- 87283-006
- 11-digit product format
- 872830006
- Labeler code
- 87283
- Product ID
- 87283-006_47df0de5-012b-c896-e063-6394a90a9cef
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AVOBENZONE ,OCTISALATE ,OCTOCRYLENE , HOMOSALATE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Aopline Biotechnology (Guangzhou) Co., Ltd.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-01-08
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 1.5; 4.5; 2.5; 3.5 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
- SUNSCREEN GLOWING
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AVOBENZONE | 1.5 g/50mL |
| HOMOSALATE | 4.5 g/50mL |
| OCTISALATE | 2.5 g/50mL |
| OCTOCRYLENE | 3.5 g/50mL |
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 |
|---|
| 87283-006-01 | SUNSCREEN GLOWING | 60 mL in 1 BOTTLE | LOTION | 60 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87283-006-01 | 87283000601 | 60 mL in 1 BOTTLE (87283-006-01) | 60 ml | 2026-01-08 | No | No | Current |