Label: CELLULAR SWISS UV PROTECTION VEIL SPF30- octocrylene, homosalate, octisalate, avobenzone cream
- NDC Code(s): 68026-809-50
- Packager: La Prairie, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 26, 2023
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- Drug Facts
- Active Ingredients
- Uses:
- Warnings:
-
Directions:
• apply daily after cleansing and toning
• smooth over face & throat
• apply liberally 15 minutes before sun exposure
• children under 6 months of age: Ask a doctor
• reapply at least every 2 hours
• use a water resistant sunscreen if swimming or sweating
• 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 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 -
Inactive Ingredients:
Water (Aqua, Glycerin, Butyloctyl Salicylate, C12-15 Alkyl Benzoate, Butylene Glycol, Microcrystalline Cellulose, Glycoproteins*, Panax Ginseng Root Extract*, Equisetum Arvense Extract*, Saccharomyces Cerevisiae Extract*, Lactobacillus Ferment*, Pinus Pinaster Bark Extract, Carnosine, Dipeptide Diaminobutyroyl Benzylamide Diacetate, Tocopherol, Ascorbic Acid, Ascorbyl Palmitate, Polyglyceryl-10 Pentastearate, Caprylic/Capric Triglyceride, Ethylhexylglycerin, C20-22 Alkyl Phosphate, Behenyl Alcohol, C20-22 Alcohol, Isodecyl Neopentanoate, Diisopropyl Sebacate, Dimethicone, Lauryl Lactate, Steareth-21, Silica Dimethyl Silylate, Cellulose Gum, Sodium Stearoyl Lactylate, Xanthan Gum, Disodium EDTA, Diethylhexyl Syringylidenemalonate, Sodium Hydroxide, PEG-8, Citric Acid, Fragrance (Parfum), Limonene, Citronellol, Alpha-Isomethyl Ionone, Geraniol, Phenoxyethanol, Potassium Sorbate, Sodium Dehydroacetate, Red 4 (CI 14700), Yellow 5 (CI 19140) i72
* La Prairie’s Exclusive Cellular Complex / Patent EP 3062763 - Other Information
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INGREDIENTS AND APPEARANCE
CELLULAR SWISS UV PROTECTION VEIL SPF30
octocrylene, homosalate, octisalate, avobenzone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68026-809 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 90 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 90 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 45 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 27 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) ASIAN GINSENG (UNII: CUQ3A77YXI) EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E) SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) MARITIME PINE (UNII: 50JZ5Z98QY) CARNOSINE (UNII: 8HO6PVN24W) DIPEPTIDE DIAMINOBUTYROYL BENZYLAMIDE DIACETATE (UNII: 38H206R00R) TOCOPHEROL (UNII: R0ZB2556P8) ASCORBIC ACID (UNII: PQ6CK8PD0R) ASCORBYL PALMITATE (UNII: QN83US2B0N) POLYGLYCERYL-10 PENTASTEARATE (UNII: PMX5872701) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) C20-22 ALKYL PHOSPHATE (UNII: L4VKP0Y7RP) DOCOSANOL (UNII: 9G1OE216XY) C20-22 ALCOHOLS (UNII: O4M0347C6A) ISODECYL NEOPENTANOATE (UNII: W60VYE24XC) DIISOPROPYL SEBACATE (UNII: J8T3X564IH) DIMETHICONE (UNII: 92RU3N3Y1O) LAURYL LACTATE (UNII: G5SU0BFK7O) STEARETH-21 (UNII: 53J3F32P58) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN) XANTHAN GUM (UNII: TTV12P4NEE) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248) SODIUM HYDROXIDE (UNII: 55X04QC32I) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) LIMONENE, (+)- (UNII: GFD7C86Q1W) .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B) GERANIOL (UNII: L837108USY) PHENOXYETHANOL (UNII: HIE492ZZ3T) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM DEHYDROACETATE (UNII: 8W46YN971G) FD&C RED NO. 4 (UNII: X3W0AM1JLX) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68026-809-50 1 in 1 BOX 08/01/2021 1 50 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 08/01/2021 Labeler - La Prairie, Inc. (606554996)
