luminous aqua sunscreen mist
- Product NDC
- 84326-724
- 11-digit product format
- 843260724
- Labeler code
- 84326
- Product ID
- 84326-724_41a6ee97-46df-889f-e063-6394a90a6d62
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- RBGROUP Co., Ltd
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-12-23
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 2.8; 7.3; 4.8; 9.5 g/100g; g/100g; g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- luminous aqua sunscreen mist
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AVOBENZONE | 2.8 g/100g |
| HOMOSALATE | 7.3 g/100g |
| OCTISALATE | 4.8 g/100g |
| OCTOCRYLENE | 9.5 g/100g |
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 |
|---|
| 84326-724-01 | luminous aqua sunscreen mist | 1 g in 1 BOTTLE, PLASTIC | SPRAY | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 84326-724 | LUMINOUS AQUA SUNSCREEN MIST (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) SPRAY [RBGROUP CO., LTD] | 1 | Current NDC, 1 package rows | 20241225_29fc0c2b-8d10-8704-e063-6394a90ad504.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84326-724-01 | 84326072401 | 1 g in 1 BOTTLE, PLASTIC (84326-724-01) | 1 g | 2024-12-23 | No | No | Current |