PURPOSE
- Product NDC
- 24208-001
- 11-digit product format
- 242080001
- Labeler code
- 24208
- Product ID
- 24208-001_22f5cdc2-86cc-7dfd-e063-6394a90a539d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate, Octisalate and Oxybenzone
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Bausch & Lomb Incorporated
- Application
- M018
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2013-10-07
- 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
- 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 |
|---|
| 24208-001-04 | PURPOSE | 113 g in 1 BOTTLE | LOTION | 113 | | 3 |
| 24208-001-04 | PURPOSE | 1 in 1 CARTON | LOTION | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 24208-001 | PURPOSE (OCTINOXATE, OCTISALATE AND OXYBENZONE) LOTION [BAUSCH & LOMB INCORPORATED] | 3 | Current NDC, Legacy NDC, 2 package rows | 20240927_a1e14135-b8da-4cee-8c5b-1893572f4de4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 24208-001-04 | 24208000104 | 1 BOTTLE in 1 CARTON (24208-001-04) / 113 g in 1 BOTTLE | 1 bottle | 2013-10-07 | 0000-00-00 | No | No | Current |