Label: GO DAILY DEFENSE SOOTHING MINERAL FACE SUNSCREEN SPF-30- zinc oxide lotion
- NDC Code(s): 73054-116-11
- Packager: SOLARA SUNCARE, INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated May 31, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- PURPOSE
- USES
- Warnings
- KEEP OUT OF REACH OF CHILDREN
-
DIRECTIONS
- shake before each use
- apply generously and evenly to face and neck 15 minutes before sun exposure
- use a water resistant sunscreen if swimming or sweating
- reapply at least every 2 hours
- Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
- limit time in the sun, especially from 10 a.m. - 2 p.m.
- wear long-sleeve shirts, pants, hats, and sunglasses
- children under 6 months: Ask a doctor
-
INACTIVE INGREDIENTS
Water (Aqua), Caprylic/Capric Triglyceride, Coconut Alkanes, Cetearyl Alcohol, Glycerin, Aloe Barbadensis Leaf Juice, Coco-Glucoside, Lactobacillus Ferment, Camellia Sinensis (Green Tea) Leaf Extract, Helianthus Annuus (Sunflower) Sprout Extract, Hydrolyzed Jojoba Esters, Butyrospermum Parkii Nut Extract, Caesalpinia Spinosa Fruit Pod Extract, Caprylhydroxamic Acid, Glyceryl Caprylate, Cetearyl Glucoside, Caprylyl/Capryl Glucoside, Coco-Caprylate/Caprate, Polyhydroxystearic Acid, Polyglyceryl-3 Polyricinoleate, Isostearic Acid, Lecithin, Dipotassium Glycyrrhizinate, Sodium Phytate, Propylene Glycol, Xanthan Gum, Sclerotium Gum, Phenoxyethanol, Sodium Benzoate, Tocopherol
- OTHER INFORMATION
- QUESTIONS OR COMMENTS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
GO DAILY DEFENSE SOOTHING MINERAL FACE SUNSCREEN SPF-30
zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73054-116 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 19 g in 100 mL Inactive Ingredients Ingredient Name Strength MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) COCONUT ALKANES (UNII: 1E5KJY107T) HELIANTHUS ANNUUS SPROUT (UNII: 4P26HG1S5W) POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4) ISOSTEARIC ACID (UNII: X33R8U0062) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) LIMOSILACTOBACILLUS FERMENTUM (UNII: 2C1F12C6AP) SODIUM BENZOATE (UNII: OJ245FE5EU) CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) CAESALPINIA SPINOSA FRUIT POD (UNII: EXY4496LWD) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) PHYTATE SODIUM (UNII: 88496G1ERL) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) CETYL ALCOHOL (UNII: 936JST6JCN) TOCOPHEROL (UNII: R0ZB2556P8) COCO GLUCOSIDE (UNII: ICS790225B) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) PHENOXYETHANOL (UNII: HIE492ZZ3T) ALOE VERA LEAF (UNII: ZY81Z83H0X) HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W) COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) BETASIZOFIRAN (UNII: 2X51AD1X3T) XANTHAN GUM (UNII: TTV12P4NEE) SHEANUT (UNII: 84H6HBP32L) GREEN TEA LEAF (UNII: W2ZU1RY8B0) GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73054-116-11 1 in 1 BOX 10/17/2021 1 50 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M020 10/17/2021 Labeler - SOLARA SUNCARE, INC. (040998319)
