OTC - ACTIVE INGREDIENT SECTION
Ethylhexyl Methoxycinnamate(Octinoxate), Ethylhexyl Salicylate(Octisalate), Titanium Dioxide, Zinc Oxide
Ethylhexyl Methoxycinnamate(Octinoxate), Ethylhexyl Salicylate(Octisalate), Titanium Dioxide, Zinc Oxide
Water, Propylene Glycol, Cyclohexasiloxane, Butylene Glycol, Polyglyceryl-4 Isostearate, PEG-10 Dimethicone, Hydrogenated Poly(C6-14 Olefin), Cetyl PEG/PPG-10/1 Dimethicone, Cetyl Ethylhexanoate, Betaine, Cyclomethicone, Magnesium Sulfate, Disteardimonium Hectorite, Methyl Methacrylate Crosspolymer, Aluminum Hydroxide, Stearic Acid, Caprylyl Glycol, Dextrin Palmitate, Dimethicone Crosspolymer, Phenyl Trimethicone, Sodium Guaiazulene Sulfonate, Glycerin, Caprylhydroxamic Acid, Allantoin, Aloe Barbadensis Leaf Juice, Perilla Ocymoides Leaf Extract, Phenoxyethanol, Biosaccharide Gum-4, Citric Acid, Potassium Sorbate, Sodium Benzoate, Fragrance
Helps prevent sunburn.
Helps improve skin tone and keep moisturized.
keep out of reach of the children
After the basic skincare routine, apply a suitable amount and gently spread.
When using this product keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if rash or irritation develops and lasts.
for external use only
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 71638-0014-1 | 2021-07-23 | C162847 | 48780-1 | c7ccaba7-19a4-fd44-e053-dadaa90aa01b | Dermafirm - LABODE DERMAFIRM SUN DEFENSE MAKE UP BASE (71638-0013) |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71638-0014-1 | LABODE DERMAFIRM SUN DEFENSE MAKE UP BASE | 30 g in 1 TUBE, WITH APPLICATOR | CREAM | 30 | 2 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 71638-0014 | LABODE DERMAFIRM SUN DEFENSE MAKE UP BASE (ETHYLHEXYL METHOXYCINNAMATE, ETHYLHEXYL SALICYLATE, TITANIUM DIOXIDE, ZINC OXIDE) CREAM [DERMAFIRM INC.] | 2 | Legacy NDC, 1 package rows | 20191204_97a9d2ca-e817-e135-e053-2a95a90ae5c1.zip |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 71638-0014 | 71638-0014-1 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| ZINC OXIDE | SOI2LOH54Z | ACTIB |
| OCTISALATE | 4X49Y0596W | ACTIB |
| TITANIUM DIOXIDE | 15FIX9V2JP | ACTIB |
| OCTINOXATE | 4Y5P7MUD51 | 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 |
|---|---|---|---|---|---|---|
| 98d7e5df-e3ad-379b-e053-2995a90a41fa | 97a9d2ca-e817-e135-e053-2a95a90ae5c1 | 2019-12-03 | Warnings | 98d7e5df-e3ad-379b-e053-2995a90a41fa 97a9d2ca-e817-e135-e053-2a95a90ae5c1 |
Adverse event summaries are temporarily unavailable. Other product information remains available.