Label: HYDRATOR PLUS SPF 30- broad spectrum lotion
- NDC Code(s): 68726-263-11, 68726-263-37, 68726-263-53
- 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: as a doctor.
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 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
Betaine
Bisabolol
Butyloctyl Salicylate
Caffeine
Ceteareth-20
Cetearyl Olivate
Citrus Aurantium Dulcis (Orange) Peel Extract
Coco-Caprylate/Caprate
Coconut Alkanes
Cyclopentasiloxane
Dimethicone
Ethylhexylgylcerin
Glycerin
Hydrolyzed Jojoba Esters
Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer
Octyldodecyl Neopentanoate
PEG-7 Trimethylolpropane Coconut Ether
Phenoxyethanol
Polyisobutene
Propanediol
Sodium Hyaluronate
Sodium PCA
Sorbitan Olivate
Tetradecane
Tocopheryl Acetate
Tremella Fuciformis Sporocarp Extract
Triethoxycaprylylsilane
Water
- Questions
- Hydrator Plus
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INGREDIENTS AND APPEARANCE
HYDRATOR PLUS SPF 30
broad spectrum lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68726-263 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 10 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 5.4 g in 100 mL Inactive Ingredients Ingredient Name Strength ORANGE PEEL (UNII: TI9T76XD44) HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W) HYALURONATE SODIUM (UNII: YSE9PPT4TH) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) LEVOMENOL (UNII: 24WE03BX2T) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) OAT BRAN (UNII: KQX236OK4U) SORBITAN OLIVATE (UNII: MDL271E3GR) COCONUT ALKANES (UNII: 1E5KJY107T) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52) CAFFEINE (UNII: 3G6A5W338E) TETRADECANE (UNII: 03LY784Y58) OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T) DIMETHICONE (UNII: 92RU3N3Y1O) COCOYL CAPRYLOCAPRATE (UNII: 8D9H4QU99H) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) TREMELLA FUCIFORMIS FRUITING BODY (UNII: GG8N28393G) PHENOXYETHANOL (UNII: HIE492ZZ3T) PROPANEDIOL (UNII: 5965N8W85T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) CETEARYL OLIVATE (UNII: 58B69Q84JO) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) BETAINE (UNII: 3SCV180C9W) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68726-263-11 50 mL in 1 TUBE; Type 0: Not a Combination Product 05/01/2020 2 NDC:68726-263-37 7.4 mL in 1 TUBE; Type 0: Not a Combination Product 05/01/2020 3 NDC:68726-263-53 195 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)
