Ultra Violette Sequin Supreme SPF 50
- Product NDC
- 84803-107
- 11-digit product format
- 848030107
- Labeler code
- 84803
- Product ID
- 84803-107_4102349b-e16f-f645-e063-6394a90a0223
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Grace and Fire USA Inc.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-11-01
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 30; 70; 50; 80 mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ultra Violette Sequin Supreme SPF 50
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AVOBENZONE | 30 mg/mL |
| HOMOSALATE | 70 mg/mL |
| OCTISALATE | 50 mg/mL |
| OCTOCRYLENE | 80 mg/mL |
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 |
|---|
| 84803-107-15 | Ultra Violette Sequin Supreme SPF 50 | 15 mL in 1 TUBE | LOTION | 15 | | 1 |
| 84803-107-50 | Ultra Violette Sequin Supreme SPF 50 | 50 mL in 1 BOTTLE | LOTION | 50 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84803-107-15 | 84803010715 | 15 mL in 1 TUBE (84803-107-15) | 15 ml | 2025-11-01 | No | No | Historical |
| 84803-107-50 | 84803010750 | 50 mL in 1 BOTTLE (84803-107-50) | 50 ml | 2025-11-01 | No | No | Historical |