Label: WEIGHTLESS PROTECTION SPF 45- sunscreen broad spectrum lotion
- NDC Code(s): 68726-262-11, 68726-262-37, 68726-262-53
- Packager: CP Skin Health Group, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 14, 2024
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- Official Label (Printer Friendly)
- Active Ingredients
- Uses
- Warnings
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Directions
Apply liberally 15 minutes before sun exposure.
Use a water resistant sunscreen if swimming or sweating
Reapply at least every two hours
Children under 6 months: ask a doctor
Sun Protectin 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 skin protecting measures including: limit time in the sun, especially from 10 a.m. - 2 p.m., wear long sleeved shirts, pants, hats and sunglasses.
- Other Information
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Inactive Ingredients
Avena Sativa (Oat) Bran Extract
Bisabolol
Butylene Glycol
Butyloctyl Salicylate
Caffeine
Caprylic/Capric Triglyceride
Caprylyl Methicone
Citrus Aurantium Dulcis (Orange) Peel Extract
Cucumis Melo Cantalupensis Fruit Extract
Cucumis Melo (Melon) Fruit Extract
Cucumis Sativus (Cucumber) Fruit Extract
Cyclopentasiloxane
Dimethicone
Ectoin
Ethyl Ferulate
Ethylhexylglycerin
Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer
Mentha Piperita (Peppermint) Extract
Mentha Viridis (Spearmint) Extract
Octyldodecyl Neopentanoate
Oleth-3 Phosphate
Passiflora Incarnata Fruit Extract
PEG-7 Trimethylolpropane Coconut Ether
Phenoxyethanol
Polyisobutene
Propanediol
Pyrus Malus (Apple) Fruit Extract
Rubus Idaeus (Raspberry) Fruit Extract
Rose Extract
Santalum Album (Sandalwood) Wood Extract
Silybum Marianum Seed Extract
Sodium Hyaluronate
Sodium Stearoyl Glutamate
Styrene/Acrylates Copolymer
Tocopheryl Acetate
Triethoxycaprylylsilane
Undecylcrylene Dimethicone
Water
- Questions
- Weightless Protection
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INGREDIENTS AND APPEARANCE
WEIGHTLESS PROTECTION SPF 45
sunscreen broad spectrum lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68726-262 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 2 g in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 8.4 g in 100 mL Inactive Ingredients Ingredient Name Strength APPLE (UNII: B423VGH5S9) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4) ECTOINE (UNII: 7GXZ3858RY) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SILYBUM MARIANUM SEED (UNII: U946SH95EE) CANTALOUPE (UNII: 8QF5D5H6UH) MUSKMELON (UNII: ZV095H5633) UNDECYLCRYLENE DIMETHICONE (10000 MW) (UNII: HA26P2LA4P) WATER (UNII: 059QF0KO0R) ORANGE PEEL (UNII: TI9T76XD44) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) HYALURONATE SODIUM (UNII: YSE9PPT4TH) OAT BRAN (UNII: KQX236OK4U) LEVOMENOL (UNII: 24WE03BX2T) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) ETHYL FERULATE (UNII: 5B8915UELW) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) DIMETHICONE (UNII: 92RU3N3Y1O) OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T) SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024) CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL) MENTHA SPICATA WHOLE (UNII: O2H83I4PUN) STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A) POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52) CUCUMBER (UNII: YY7C30VXJT) PASSIFLORA INCARNATA FRUIT (UNII: SF206I8G4P) PROPANEDIOL (UNII: 5965N8W85T) CAFFEINE (UNII: 3G6A5W338E) MENTHA X PIPERITA WHOLE (UNII: 79M2M2UDA9) SANDALWOOD (UNII: 3641YW25N2) RASPBERRY (UNII: 4N14V5R27W) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68726-262-11 50 mL in 1 TUBE; Type 0: Not a Combination Product 05/01/2020 2 NDC:68726-262-37 7.4 mL in 1 TUBE; Type 0: Not a Combination Product 05/01/2020 3 NDC:68726-262-53 195 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 05/01/2020 Labeler - CP Skin Health Group, Inc. (611921669)