Tula Skincare Radiant Skin Brightening Serum Skin Tint Broad Spectrum SPF 30
- Product NDC
- 84126-138
- 11-digit product format
- 841260138
- Labeler code
- 84126
- Product ID
- 84126-138_36b16cdd-8ca9-c05a-e063-6294a90a0c8c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, and Octisalate
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- The Procter & Gamble Manufacturing Company
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-06-02
- Substance
- AVOBENZONE; OCTISALATE
- Active strength
- 3; 5 g/100mL; g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
openFDA Listing Details
- Product ID
- 84126-138_36b16cdd-8ca9-c05a-e063-6294a90a0c8c
- Product type
- HUMAN OTC DRUG
- Finished product
- Yes
- Brand name base
- Tula Skincare Radiant Skin Brightening Serum Skin Tint Broad Spectrum SPF 30
- Brand name suffix
- 17 Medium Tan-Neutral
- Generic name
- Avobenzone, and Octisalate
- Dosage form
- LIQUID
- Route
- TOPICAL
- Marketing start
- 2025-06-02
- Marketing category
- OTC MONOGRAPH DRUG
- Application number
- M020
- Listing expiration
- 2026-12-31
openFDA Active Ingredients
| Ingredient | Strength |
|---|
| AVOBENZONE | 3 g/100mL |
| OCTISALATE | 5 g/100mL |
openFDA Harmonized Identifiers
| Field | Values |
|---|
| Unii | 4X49Y0596W, G63QQF2NOX |
| Spl Set Id | 366144c4-ec80-e435-e063-6394a90aba54 |
| Manufacturer Name | The Procter & Gamble Manufacturing Company |
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| G63QQF2NOX | AVOBENZONE | 70356-09-1 | AVOBENZONE |
| 4X49Y0596W | OCTISALATE | 118-60-5 | OCTISALATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84126-138-30 | 84126013830 | 1 TUBE in 1 CARTON (84126-138-30) / 30 mL in 1 TUBE | 1 tube | 2025-06-02 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Avobenzone, and Octisalate | The Procter & Gamble Manufacturing Company | 2025-06-03 | HUMAN OTC DRUG LABEL | 2 |