Ultra Light Invisible SPF 40 sunscreen
- Product NDC
- 84190-001
- 11-digit product format
- 841900001
- Labeler code
- 84190
- Product ID
- 84190-001_4d299ace-531b-b044-e063-6294a90ae21d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Homosalate 8%, Octisalate 5.0%, Avobenzone 3.0%, Octocrylene 4.0%
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- RK Shea LLC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-12-01
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 3; 8; 5; 4 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
- Ultra Light Invisible SPF 40 sunscreen
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AVOBENZONE | 3 g/100mL |
| HOMOSALATE | 8 g/100mL |
| OCTISALATE | 5 g/100mL |
| OCTOCRYLENE | 4 g/100mL |
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 |
|---|
| 84190-001-02 | Ultra Light Invisible SPF 40 sunscreen | 1 in 1 CARTON | GEL | 1 | | 2 |
| 84190-001-02 | Ultra Light Invisible SPF 40 sunscreen | 50 mL in 1 TUBE | GEL | 50 | | 2 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84190-001-02 | 84190000102 | 1 TUBE in 1 CARTON (84190-001-02) / 50 mL in 1 TUBE | 1 tube | 2025-12-01 | No | No | Historical |