NDC | 61369-201-12, 61369-201-14, 61369-201-32 |
Set ID | 63fec681-5957-49cc-8b9e-97c4819ce097 |
Category | HUMAN OTC DRUG LABEL |
Packager | CoLabs Intl. Corp |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- ACTIVE INGREDIENTS
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- STOP USE
- DOSAGE & ADMINISTRATION
-
OTHER SAFETY INFORMATION
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:
- LIMIT TIME IN THE SUN, ESPECIALLY FROM 10 A.M. - 2 P.M.
- WEAR LONG-SLEEVED SHIRTS, PANTS, HATS, AND SUNGLASSES
- CHILDREN UNDER 6 MONTHS: ASK A DOCTOR.
OTHER INFORMATION
- PROTECT THE PRODUCT IN THIS CONTAINER FROM EXCESSIVE HEAT AND DIRECT SUNLIGHT.
-
INACTIVE INGREDIENTS
Water (Aqua), Caprylic/Capric Triglyceride, Acrylates Copolymer, Dimethicone, Vinyldimethyl/Trimethylsiloxysilicate/Dimethicone Crosspolymer, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Isohexadecane, Polysorbate 80, Polysorbate 20, Sorbitan Monooleate, Cocodimonium Hydroxypropyl Hydrolyzed Keratin, Butyrospermum Parkii (Shea) Oil, Polyamide 3, Carboxymethylcellulose Na,
Ethylenediamine/Stearyl Dimer Dilinoleate Copolymer, PG Hydroxyethylcellulose Stearyldimonium Chloride, Sodium Lauryl Glucose Carboxylate, Lauryl Glucoside, Laurdimoniumhydroxypropyl Decylglucosides Chloride, Gellan Gum, Sodium Alginate, Carrageenan, Tocopheryl Acetate, Rubeus Idaeus (Red Raspberry) Oil, Punica Granatum (Pomegranate) Seed Oil, Camellia Oleifera (Organic Green Tea) Seed Oil, Arctium Lappa Root Extract (Burdock Root), Phenoxyethanol, Trimethoxybenzylidene Pentanedione, Caprylyl Glycol - QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
KLENSKIN BROAD SPECTRUM SPF-50
avobenzone, octocrylene, octinoxate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61369-201 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 2.1 g in 100 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 5.4 g in 100 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 5 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L) DIMETHICONE (UNII: 92RU3N3Y1O) VINYLDIMETHYL/TRIMETHYLSILOXYSILICATE STEARYL DIMETHICONE CROSSPOLYMER (UNII: 01S784FLCO) SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX) ISOHEXADECANE (UNII: 918X1OUF1E) POLYSORBATE 80 (UNII: 6OZP39ZG8H) POLYSORBATE 20 (UNII: 7T1F30V5YH) SORBITAN MONOOLEATE (UNII: 06XEA2VD56) HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL) SHEANUT OIL (UNII: O88E196QRF) POLYAMIDE-3 (12000 MW) (UNII: L7P3YWF22X) CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) ETHYLENEDIAMINE (UNII: 60V9STC53F) DIISOSTEARYL DIMER DILINOLEATE (UNII: 04P17590AP) HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP) DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X) SODIUM LAURYL GLYCOL CARBOXYLATE (UNII: 8L0472VMYL) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) LAURDIMONIUMHYDROXYPROPYL DECYLGLUCOSIDE CHLORIDE (UNII: GCO3569D5L) GELLAN GUM (LOW ACYL) (UNII: 7593U09I4D) SODIUM ALGINATE (UNII: C269C4G2ZQ) CARRAGEENAN (UNII: 5C69YCD2YJ) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) RASPBERRY SEED OIL (UNII: 9S8867952A) POMEGRANATE SEED OIL (UNII: 0UI45XV0T6) CAMELLIA SINENSIS SEED OIL (UNII: O5R6DK2M9K) ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) TRIMETHOXYBENZYLIDENE PENTANEDIONE (UNII: 322V0ACF25) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61369-201-12 56 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/16/2016 2 NDC:61369-201-14 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/27/2016 3 NDC:61369-201-32 946 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/10/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 04/16/2016 Labeler - CoLabs Intl. Corp (829850879)