Sunscreen
- Product NDC
- 72239-001
- 11-digit product format
- 722390001
- Labeler code
- 72239
- Product ID
- 72239-001_b7ceac19-93b5-1ea6-e053-2995a90a14e5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octocrylene, Octisalate, Avobenzone
- Dosage form
- AEROSOL, SPRAY
- Route
- TOPICAL
- Labeler
- OL Products, Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-10-12
- Marketing end
- 0000-00-00
- Substance
- OCTOCRYLENE; AVOBENZONE; OCTISALATE
- Active strength
- 2 g/100g; g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72239-001-01 | Sunscreen | 241 g in 1 BOTTLE, SPRAY | AEROSOL, SPRAY | 241 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72239-001 | SUNSCREEN (OCTOCRYLENE, OCTISALATE, AVOBENZONE) AEROSOL, SPRAY [OL PRODUCTS, INC.] | 4 | Legacy NDC, 1 package rows | 20210101_676335de-4a14-f8d7-e053-2a91aa0ab97c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72239-001-01 | 72239000101 | 241 g in 1 BOTTLE, SPRAY (72239-001-01) | 241 g | 2018-10-12 | 0000-00-00 | No | No | Current |