Label: GLO SKIN BEAUTY OIL FREE SPF 40 lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 60541-1000-5 - Packager: Hayden Caleel LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated December 18, 2017
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- Official Label (Printer Friendly)
- Active Ingredients
- Uses
- Warnings
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Directions
• apply generously 15 minutes before sun exposure
• 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-sleeved shirts, pants, hats, and sunglasses
• children under 6 months of age: Ask a doctor -
Inactive ingredients
Aqua/Water/Eau, Isopropyl Palmitate, Ethylhexyl Stearate, Ethylhexyl Isononanoate, Cyclopentasiloxane, Cetearyl Glucoside, Dimethicone, Phenoxyethanol, Glycereth-26, Oleth-3 Phosphate, Allantoin, Triethoxycaprylylsilane, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Polyisobutene, Panthenol, Butylene Glycol, PEG-7 Trimethylolpropane Coconut Ether, Sodium Hyaluronate, Tocopheryl Acetate, Ascorbyl Palmitate, Iodopropynyl Butylcarbamate
- Other Information
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INGREDIENTS AND APPEARANCE
GLO SKIN BEAUTY OIL FREE SPF 40
glo skin beauty oil free spf 40 lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60541-1000 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 7.5 g in 100 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 2.5 g in 100 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 7.5 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5) ETHYLHEXYL ISONONANOATE (UNII: I6KB4GE3K4) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) DIMETHICONE (UNII: 92RU3N3Y1O) PHENOXYETHANOL (UNII: HIE492ZZ3T) GLYCERETH-26 (UNII: NNE56F2N14) OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL) ALLANTOIN (UNII: 344S277G0Z) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PANTHENOL (UNII: WV9CM0O67Z) ASCORBYL PALMITATE (UNII: QN83US2B0N) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60541-1000-5 1 in 1 CARTON 12/31/2017 1 50 g 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 final part352 12/31/2017 Labeler - Hayden Caleel LLC (011367468)
