Label: SNOWSKIN SUNSCREEN- octinoxate, oxybenzone, titanium dioxide, zinc oxide cream
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Contains inactivated NDC Code(s)
NDC Code(s): 75916-4018-1, 75916-4018-4 - Packager: Skin Alive, Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 January 5, 2011
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
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PRINCIPAL DISPLAY PANEL
spf30+
Very water/sweat resistant
broad spectrum
UVA/UVB
SNOWSKIN Sunscreen
Proven in Extreme New Zealand conditions
4.2 fl oz (125 ml)
manuka honey UMF 18
contains no nanoparticles - Aminobenzoic acid (PABA) Free
Snowskin SPF 30+ Sunscreen, Very water/sweat resistant, broad spectrum, UVA/UVB Protection. keep your "Skin alive" with this non-greasy sweat-resistant formula that won't run into your eyes, leaving you free to focus on what really matters. Whether you're up on the hill or deep in the trees, Snowskin offers great protection from the elements.
Expires:
Lot Number:
www.snowskin.co
DIST BY Quiver Dist., Bend Oregon, USA 97701
MADE IN NZ
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SNOWSKIN SUNSCREEN
octinoxate, oxybenzone, titanium dioxide, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75916-4018 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 7.5 mL in 100 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 3.45 mL in 100 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 1 mL in 100 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC OXIDE 1.95 mL in 100 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CYCLOMETHICONE (UNII: NMQ347994Z) WATER (UNII: 059QF0KO0R) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYSORBATE 60 (UNII: CAL22UVI4M) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75916-4018-4 125 mL in 1 TUBE 2 NDC:75916-4018-1 40 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 01/05/2011 Labeler - Skin Alive, Ltd. (593384746)