Byoma Ultralight Face Fluid SPF 50
- Product NDC
- 84821-003
- 11-digit product format
- 848210003
- Labeler code
- 84821
- Product ID
- 84821-003_26591cef-9dae-ac10-e063-6394a90ad72e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- BYOMA LIMITED
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-01-01
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 30; 70; 50; 90 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
- Byoma Ultralight Face Fluid SPF 50
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AVOBENZONE | 30 mg/mL |
| HOMOSALATE | 70 mg/mL |
| OCTISALATE | 50 mg/mL |
| OCTOCRYLENE | 90 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 |
|---|
| 84821-003-50 | Byoma Ultralight Face Fluid SPF 50 | 50 mL in 1 BOTTLE, PLASTIC | LOTION | 50 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 84821-003 | BYOMA ULTRALIGHT FACE FLUID SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [BYOMA LIMITED] | 2 | Current NDC, 1 package rows | 20241109_2658df86-8cbb-83dd-e063-6394a90ac4e8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84821-003-50 | 84821000350 | 50 mL in 1 BOTTLE, PLASTIC (84821-003-50) | 50 ml | 2024-01-01 | No | No | Current |