AL0038200 Alba VE Sunscreen Kids SPF50
- Product NDC
- 61995-2382
- 11-digit product format
- 619952382
- Labeler code
- 61995
- Product ID
- 61995-2382_ba9fb048-658d-6f48-e053-2995a90a3ea9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Homosalate, Octocrylene, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- The Hain Celestial Group, Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2015-02-03
- Marketing end
- 0000-00-00
- Substance
- OCTOCRYLENE; OCTISALATE; AVOBENZONE; HOMOSALATE
- Active strength
- 8 g/100g; g/100g; g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61995-2382-6 | AL0038200 Alba VE Sunscreen Kids SPF50 | 177 g in 1 BOTTLE, SPRAY | SPRAY | 177 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61995-2382 | AL0038200 ALBA VE SUNSCREEN KIDS SPF50 (HOMOSALATE, OCTOCRYLENE, ETHYLHEXYL SALICYLATE, BUTYL METHOXYDIBENZOYLMETHANE) SPRAY [THE HAIN CELESTIAL GROUP, INC.] | 3 | Legacy NDC, 1 package rows | 20210207_2669183c-7a5e-037e-e054-00144ff88e88.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61995-2382-6 | 61995238206 | 177 g in 1 BOTTLE, SPRAY (61995-2382-6) | 177 g | 2015-02-03 | 0000-00-00 | No | No | Current |