Arizona Sun Sunscreen SPF 8
- Product NDC
- 61973-100
- 11-digit product format
- 619730100
- Labeler code
- 61973
- Product ID
- 61973-100_4f0c8f3f-68e2-8c30-e063-6394a90a6805
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sunscreen
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Arizona Sun Products
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-02-02
- Substance
- OCTINOXATE; OCTISALATE; OXYBENZONE
- Active strength
- 65; 10; 10 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
- Arizona Sun Sunscreen SPF 8
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OCTINOXATE | 65 mg/g |
| OCTISALATE | 10 mg/g |
| OXYBENZONE | 10 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4Y5P7MUD51, 4X49Y0596W, 95OOS7VE0Y |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61973-100-04 | Arizona Sun Sunscreen SPF 8 | 120 g in 1 BOTTLE | LOTION | 120 | | 4 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 61973-100-04 | 61973010004 | 120 g in 1 BOTTLE (61973-100-04) | 120 g | 2024-02-02 | No | No | Current |