Ulta Beauty
- Product NDC
- 13630-0214
- 11-digit product format
- 136300214
- Labeler code
- 13630
- Product ID
- 13630-0214_d5e2a2f1-b7de-48e2-e053-2995a90a9b5a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octisalate, and Octocrylene
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Prime Packaging Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-03-11
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 25 mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 13630-0214-4 | Ulta BeautySPF 50 Broad Spectrum Sunscreen | 187 mL in 1 CAN | SPRAY | 187 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 13630-0214 | ULTA BEAUTY SPF 50 BROAD SPECTRUM SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE) SPRAY [PRIME PACKAGING INC.] | 1 | Legacy NDC, 1 package rows | 20220119_d5e2a336-8c5c-1911-e053-2a95a90a7272.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 13630-0214-4 | 13630021404 | 187 mL in 1 CAN (13630-0214-4) | 187 ml | 2021-03-11 | 0000-00-00 | No | No | Current |