Sunscreen
- Product NDC
- 72239-002
- 11-digit product format
- 722390002
- Labeler code
- 72239
- Product ID
- 72239-002_b7ced1e8-2607-e9fa-e053-2995a90a6637
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SELFIE SPF30 Spray Lotion
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- O.L. Products, Inc,
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-07-09
- Marketing end
- 0000-00-00
- Substance
- HOMOSALATE; OCTOCRYLENE; OCTISALATE; AVOBENZONE
- Active strength
- 4 g/36g; g/36g; g/36g; g/36g
- 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 |
|---|
| 72239-002-01 | Sunscreen | 234 g in 1 BOTTLE, SPRAY | SPRAY | 234 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72239-002 | SUNSCREEN (SELFIE SPF30 SPRAY LOTION) SPRAY [O.L. PRODUCTS, INC,] | 3 | Legacy NDC, 1 package rows | 20210101_6a1f637d-3b3d-9714-e053-2a91aa0a5abc.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72239-002-01 | 72239000201 | 234 g in 1 BOTTLE, SPRAY (72239-002-01) | 234 g | 2018-07-09 | 0000-00-00 | No | No | Current |