KLENSKIN SHOWERON SUNSCREEN  SPF-30- avobenzone, octocrylene, octinoxate gel 
CoLabs Intl. Corp

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.

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COLABS - Klenskin Wash On Shampoo, Face & Body Wash SPF 30, Fragrance Free (61369-101)

ACTIVE INGREDIENTS

AVOBENZONE 2.75%

OCTOCRYLENE 7.04%

OCTINOXATE 7.2%

PURPOSE

SUNSCREEN

USES

WARNINGS

KEEP OUT OF REACH OF CHILDREN. IF PRODUCT IS SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

STOP USE AND ASK A DOCTOR IF RASH OR IRRITATION DEVELOPS.

DIRECTIONS

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

OTHER INFORMATION

INACTIVE INGREDIENTS

WATER, SODIUM LAURETH SULFATE, SODIUM LAURYL SULFATE, COCAMIDOPROPYL BETAINE, POLYSORBATE 20, GLYCERIN, POLYQUATERNIUM-10, SORBITAN MONOOLEATE, COCODIMONIUM HYDROXYPROPYL HYDROLYZED KERATIN, BUTYROSPERMUM PARKII (SHEA) OIL, DIMETHICONE, POLYAMIDE-3, SORBITAN STEARATE, CARBOXYMETHYCELLULOSE NA, ETHYLENEDIAMINE/STEARYL DIMER DILINOLEATE COPOLYMER, PG HYDROXYETHYLCELLULOSE STEARDIMONIUM CHLORIDE, SODIUM LAURYL GLUCOSE CARBOXYLATE, PHENOXYETHANOL, ACRYLATES/C12-22 ALKYL METHACRYLATE COPOLYMER, CAPRYLYL GLYCOL, TETRASODIUM EDTA, LAURYLDIMONIUMHYDROXYPROPYL DECYLGLUCOSIDES CHLORIDE, GELLAN GUM, SODIUM ALGINATE, ARCTIUM LAPPA (BURDOCK ROOT) EXTRACT, LAURYL GLUCOSIDE, CAMELIA OLEIFERA (GREEN TEA) SEED OIL, PUNICA GRANATUM (POMEGRANATE) SEED OIL, RUBEUS IDAEUS (RED RASPBERRY) OIL, VACCINIUM MACROCARPON (CRANBERRY) SEED OIL, VITIS VINIFERA (GRAPE) SEED OIL, CARRAGEENAN, CITRIC ACID, SODIUM CHLORIDE

QUESTIONS OR COMMENTS? PLEASE CALL TOLL FREE 888.878.5536

8oz-klenskin_EXP_LBL

KLENSKIN SHOWERON SUNSCREEN   SPF-30
avobenzone, octocrylene, octinoxate gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61369-101
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE2.75 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE7.04 g  in 100 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE7.2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYQUATERNIUM-10 (125 MPA.S AT 2%) (UNII: L45WU8S981)  
SORBITAN MONOOLEATE (UNII: 06XEA2VD56)  
HYDROLYZED BOVINE ELASTIN (BASE; 1000 MW) (UNII: ZR28QKN0WT)  
SHEANUT OIL (UNII: O88E196QRF)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)  
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)  
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
DILINOLEIC ACID/ETHYLENEDIAMINE COPOLYMER (UNII: OC72DYI76F)  
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)  
DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)  
SODIUM LAURYL GLYCOL CARBOXYLATE (UNII: 8L0472VMYL)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
EDETATE SODIUM (UNII: MP1J8420LU)  
HYDROXYETHYL LAURDIMONIUM CHLORIDE (UNII: 8467K53E3Y)  
GELLAN GUM (LOW ACYL) (UNII: 7593U09I4D)  
SODIUM ALGINATE (UNII: C269C4G2ZQ)  
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)  
CAMELLIA OLEIFERA SEED (UNII: 59ED29FM2J)  
POMEGRANATE SEED OIL (UNII: 0UI45XV0T6)  
RASPBERRY SEED OIL (UNII: 9S8867952A)  
CRANBERRY SEED OIL (UNII: 73KDS3BW5E)  
GRAPE SEED OIL (UNII: 930MLC8XGG)  
CARRAGEENAN (UNII: 5C69YCD2YJ)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:61369-101-18236 mL in 1 BOTTLE; Type 0: Not a Combination Product07/28/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35207/28/2014
Labeler - CoLabs Intl. Corp (829850879)

Revised: 2/2022
Document Id: d8288a2c-dc92-cc66-e053-2a95a90a7c4e
Set id: 00d73e47-97fd-4fe7-80d4-bf19ed0c9dda
Version: 10
Effective Time: 20220216
 
CoLabs Intl. Corp