OTC - ACTIVE INGREDIENT SECTION
Active Ingredients:
Zinc Oxide 18.6%
Active Ingredients:
Zinc Oxide 18.6%
Purpose:
Sunscreen
Uses:
Warnings:
For external use only
When using this product
Keep out of reach of childrean
Inactive Ingredients:
Water (Aqua), Caprylic/Capric Triglyceride, Glyceryl Stearate, PEG 100 Stearate, Sorbitan Stearate, Citric Acid, Imperata Cylidrica Root Extract, Tocopheryl Linoleate, Lecithin, Xanthan Gum, PEG 8, Ascorbic Acid, Ethylhexylglycerin, Sodium Lactate, Micrococcus Lysate, Arabidopsis Extract, Plankton Extract, Teprenone, Phoenix dactylifera (date) extract, Laureth-7, Disodium EDTA, Dipotassium Glycyrrhizte, Caprylyl Glycol, Tocopherol, Ascorbyl Palmitate, Carbomer
Distributor:
Image International
Palm Beach, FL 33411 USA
Image of the product:
SUN Solar Defense Oil-free Gel SPF 30
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 62742-4040-1 | 2019-10-21 | C162847 | 48780-1 | 956f9ecf-c0cf-621f-e053-dbdaa90a74ad | Drug Facts |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62742-4040-1 | SUN Solar Defense Oil-free SPF 30 | 118 mL in 1 TUBE | GEL | 118 | 1 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 62742-4040 | SUN SOLAR DEFENSE OIL-FREE SPF 30 (ZINC OXIDE ) GEL [ALLURE LABS, INC.] | 1 | Legacy NDC, 1 package rows | 20100707_25bdc052-9c57-4bcd-a504-1b0434619003.zip |
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| ZINC OXIDE | ACTIVE INGREDIENT | SOI2LOH54Z | 1 | |
| ZINC OXIDE | ACTIVE MOIETY | SOI2LOH54Z | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 62742-4040 | 62742-4040-1 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ZINC OXIDE | SOI2LOH54Z | ACTIB |
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| e091db7c-bb5c-4180-a20b-67f7bd20125f | 25bdc052-9c57-4bcd-a504-1b0434619003 | 2010-07-02 | Warnings | e091db7c-bb5c-4180-a20b-67f7bd20125f 25bdc052-9c57-4bcd-a504-1b0434619003 |
Adverse event summaries are temporarily unavailable. Other product information remains available.