Label: DAILY DEFENSE SPF 50- face sunscreen lotion
- NDC Code(s): 68726-265-11, 68726-265-37
- 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
-
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 informaiton
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Inactive ingredients
Avena Sativa (Oat) Bran Extract
Bisabolol
Butylene Glycol
Butyloctyl Salicylate
Caffeine
Caprylyl Methicone
Citrus Aurantium Dulcis (Orange) Peel Extract
Cyclopentasiloxane
Ectoin
Ethyl Ferulate
Ethylhexylglycerin
Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer
Octyldodecyl Neopentanoate
Oleth-3 Phosphate
PEG-7 Trimethylolpropane Coconut Ether
Phenoxyethanol
Polyisobutene
Propanediol
Silybum Marianum Seed Extract
Sodium Hyaluronate
Sodium Stearoyl Glutamate
Tocopheryl Acetate
Triethoxycaprylylsilane
Water
- Questions or Comments?
- Daily Defense
-
INGREDIENTS AND APPEARANCE
DAILY DEFENSE SPF 50
face sunscreen lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68726-265 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 9.1 g in 100 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 10 g in 100 mL Inactive Ingredients Ingredient Name Strength CAFFEINE (UNII: 3G6A5W338E) OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ETHYL FERULATE (UNII: 5B8915UELW) CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T) WATER (UNII: 059QF0KO0R) ORANGE PEEL (UNII: TI9T76XD44) HYALURONATE SODIUM (UNII: YSE9PPT4TH) PROPANEDIOL (UNII: 5965N8W85T) ECTOINE (UNII: 7GXZ3858RY) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4) POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52) SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024) LEVOMENOL (UNII: 24WE03BX2T) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) MILK THISTLE (UNII: U946SH95EE) OAT BRAN (UNII: KQX236OK4U) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68726-265-11 50 mL in 1 TUBE; Type 0: Not a Combination Product 05/01/2020 2 NDC:68726-265-37 7.4 mL in 1 TUBE; 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)
