SOLBAR SUNSCREEN 50 FIFTY
- Product NDC
- 0096-0693
- 11-digit product format
- 000960693
- Labeler code
- 0096
- Product ID
- 0096-0693_48fef521-1b25-d0d5-e063-6394a90ac7b1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SUNSCREEN
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Person and Covey
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-01-22
- Substance
- AVOBENZONE; OCTINOXATE; OCTOCRYLENE; OXYBENZONE
- Active strength
- 10; 75; 100; 60 mg/g; mg/g; mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- SOLBAR SUNSCREEN 50 FIFTY
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AVOBENZONE | 10 mg/g |
| OCTINOXATE | 75 mg/g |
| OCTOCRYLENE | 100 mg/g |
| OXYBENZONE | 60 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | G63QQF2NOX, 4Y5P7MUD51, 5A68WGF6WM, 95OOS7VE0Y |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0096-0693-03 | SOLBAR SUNSCREEN 50 FIFTY | 90 g in 1 TUBE | CREAM | 90 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0096-0693-03 | 00096069303 | 90 g in 1 TUBE (0096-0693-03) | 90 g | 2026-01-22 | No | No | Historical |