SKINSUIT LIP SPF 30- zinc oxide gel 
Skin Authority LLC

----------

Skin Authority - SKINSUIT LIP SPF-30 (46007-205)

ACTIVE INGREDIENT

ZINC OXIDE 10%

PURPOSE

SUNSCREEN

USES

WARNINGS

FOR EXTERNAL USE ONLY.

DO NOT USE ON

WHEN USING THIS PRODUCT

STOP USE AND ASK A DOCTOR IF

KEEP OUT OF REACH OF CHILDREN.

SUN PROTECTION MEASURES:

SPENDING TIME IN THE SUN INCREASES YOUR RISK OF SKIN CANCER AND EARLY SKIN AGING. TO DECREASE RISK, REGULARLY USE A SUNSCREEN WITH BROAD SPECTRUM SPF VALUE OF 15+ AND OTHER SUN PROTECTION MEASURES

DIRECTIONS

APPLY EVENLY TO UPPER AND LOWER LIP 15 MINUTES BEFORE EXPOSURE. NATURAL TINT WILL ABSORB AND BECOME SHEER.

HYDROGENATED POLY(C6-14 OLEFIN), SQUALANE, BUTYLOCTYL SALICYLATE, CETEARYL DIMETHICONE, ISODODECANE, ETHYLENE/PROPYLENE/STYRENE COPOLYMER, CAPRYLYL METHICONE, SYNTHETIC FLUORPHLOGOPITE, IRON OXIDE, LECITHIN, BUTYLENE/ETHYLENE/STYRENE COPOLYMER, CAPRYLYL GLYCOL, DIMETHICONE, DIMETHICONOL/PROPYLSILSESQUIOXANE/SILICATE CROSSPOLYMER, PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE, PHENYLPROPANOL, PROPANEDIOL, TIN OXIDE, TITANIUM DIOXIDE (CI 77891), TOCOPHEROL.

OTHER INFORMATION

PROTECT THIS PRODUCT FROM EXCESSIVE HEAT AND DIRECT SUN. STORE AT 40° - 95°F (5° - 35°C).

QUESTIONS?

1-866-325-7546

MONDAY - FRIDAY (9 A.M. TO 5 P.M. PST)

0-LBL_SkinSuit Face SPF-50

SKINSUIT LIP  SPF 30
zinc oxide gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:46007-205
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION10 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
HYDROGENATED POLY(C6-14 OLEFIN; 2 CST) (UNII: P0TX083987)  
SQUALANE (UNII: GW89575KF9)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
CETEARYL METHICONE (15000 MW) (UNII: VY9RTR7MSY)  
ISODODECANE (UNII: A8289P68Y2)  
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
DIMETHICONOL/PROPYLSILSESQUIOXANE/SILICATE CROSSPOLYMER (450000000 MW) (UNII: 9KB5R958PB)  
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)  
PHENYLPROPANOL (UNII: 0F897O3O4M)  
PROPANEDIOL (UNII: 5965N8W85T)  
STANNIC OXIDE (UNII: KM7N50LOS6)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
TOCOPHEROL (UNII: R0ZB2556P8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:46007-205-113.2 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product01/02/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02001/02/2020
Labeler - Skin Authority LLC (136549396)

Revised: 10/2023
Document Id: 06fe55f3-566e-1955-e063-6394a90a1291
Set id: cb24d714-f6cd-4518-b146-627cfe6c2ccd
Version: 5
Effective Time: 20231005
 
Skin Authority LLC