Label: SOLVADERM DERMAXSOL DERMAL DEFENSE MOISTURIZER SPF-30- octocrylene, zinc oxide cream
- NDC Code(s): 84197-467-00
- Packager: SOLVADERM LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated March 21, 2024
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- DRUG FACTS
- ACTIVE INGREDIENTS:
- USES:
- WARNINGS:
-
DIRECTIONS:
Apply to all skin exposed to the sun.
*Apply liberally and evenly 15 minutes before sun exposure.
*Reapply at least every 2 hours.
*Use a water-resistant sunscreen if swimming or sweating.
*If pregnant or breast-feeding, ask a health care professional before use.
*For children under 6 months of age: Ask a doctor.
-
INACTIVE INGREDIENTS:
Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aluminum Starch Octenyl succinate, Aqua (Deionized Water), Beeswax, Calendula Officinalis Extract, Camellia Sinensis (Green Tea) Extract, Chamomilla Matricaria Extract, Cetearyl Alcohol, Cyclopentasiloxane, Diisopropyl Adipate, Dimethicone, Dimethiconol, Ethylhexylglycerin, Glycerin, Glyceryl Laurate, Glyceryl Stearate, Hyaluronic Acid, C13-14 Isoparaffin, Laureth-7, Parfum (Fragrance)., PEG-100 Stearate, Phenoxyethanol, Polyacrylamide, Sorbitan Stearate, Stearyl Alcohol, Tocopheryl Acetate (Vitamin E).
- OTHER INFORMATION:
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
SOLVADERM DERMAXSOL DERMAL DEFENSE MOISTURIZER SPF-30
octocrylene, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84197-467 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 100 mg in 1 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 70 mg in 1 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) WATER (UNII: 059QF0KO0R) YELLOW WAX (UNII: 2ZA36H0S2V) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) GREEN TEA LEAF (UNII: W2ZU1RY8B0) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) DIISOPROPYL ADIPATE (UNII: P7E6YFV72X) DIMETHICONE (UNII: 92RU3N3Y1O) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL LAURATE (UNII: Y98611C087) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) HYALURONIC ACID (UNII: S270N0TRQY) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) LAURETH-7 (UNII: Z95S6G8201) PEG-100 STEARATE (UNII: YD01N1999R) PHENOXYETHANOL (UNII: HIE492ZZ3T) SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84197-467-00 1 in 1 BOX 03/04/2024 1 50 g in 1 JAR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 03/04/2024 Labeler - SOLVADERM LLC (093262409)