Purpose Dual Treatment SPF 10
- Product NDC
- 87033-2000
- 11-digit product format
- 870332000
- Labeler code
- 87033
- Product ID
- 87033-2000_3d7fe711-a672-df30-e063-6394a90afbbf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate 7.5%, Octisalate 5%, Oxybenzone 3%
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Elysium Consumer Healthcare LLC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-08-29
- Substance
- OCTINOXATE; OCTISALATE; OXYBENZONE
- Active strength
- 7.5; 5; 3 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
- Purpose Dual Treatment SPF 10
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OCTINOXATE | 7.5 g/100g |
| OCTISALATE | 5 g/100g |
| OXYBENZONE | 3 g/100g |
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 |
|---|
| 87033-2000-1 | Purpose Dual Treatment SPF 10 | 1 in 1 CARTON | LOTION | 1 | | 1 |
| 87033-2000-1 | Purpose Dual Treatment SPF 10 | 113 g in 1 BOTTLE, PLASTIC | LOTION | 113 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 87033-2000-1 | 87033200001 | 1 BOTTLE, PLASTIC in 1 CARTON (87033-2000-1) / 113 g in 1 BOTTLE, PLASTIC | 2025-08-29 | No | No | Current |