HAMPTON SUN SPF50 SUNSHIELD BODY GLOW
- Product NDC
- 87170-010
- 11-digit product format
- 871700010
- Labeler code
- 87170
- Product ID
- 87170-010_49d8d864-063b-8c16-e063-6294a90a279a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Homosalate 10% Octocrylene 10% Avobenzone 3% Octicalate 5%
- Dosage form
- OIL
- Route
- TOPICAL
- Labeler
- S&C Hampton Sun LLC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-01-01
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 3; 10; 5; 10 g/100mL; g/100mL; g/100mL; g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- HAMPTON SUN SPF50 SUNSHIELD BODY GLOW
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AVOBENZONE | 3 g/100mL |
| HOMOSALATE | 10 g/100mL |
| OCTISALATE | 5 g/100mL |
| OCTOCRYLENE | 10 g/100mL |
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 |
|---|
| 87170-010-04 | HAMPTON SUN SPF50 SUNSHIELD BODY GLOW | 100 mL in 1 TUBE | OIL | 100 | | 2 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87170-010-04 | 87170001004 | 100 mL in 1 TUBE (87170-010-04) | 100 ml | 2026-01-01 | No | No | Current |