Label: EVERYDAYHUMANS ROSE FROM ABOVE SPF 35 SUNSCREEN BASE- zinc oxide lotion
- NDC Code(s): 72098-006-01
- Packager: EVERYDAY GROUP LIMITED
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 15, 2023
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Uses
- Warnings
-
Directions
- Shake well before use
- Apply liberally 15 minutes before sun exposure
- Use a water resistant sunscreen if swimming or sweating
- Reapply at least every 2 hours
- Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: Sun Protection Measures:
- Limit time in the sun, especially from 10 a.m to 2 p.m.
- Wear long-sleeved shirts, pants, hats, and sunglasses
- Children under 6 months of age: Ask a doctor
-
Inactive Ingredients
Water(Aqua), Butyloctyl Salicylate, Cocos Nucifera (Coconut) Oil, Diheptyl Succinate, Capryloyl Glycerin/Sebacic Acid Copolymer, Cetearyl Alcohol, Sodium Stearoyl Glutamate, Butyrospermum Parkii (Shea) Butter, Polyhydroxystearic Acid, Microcrystalline Cellulose, Squalane, Glycerin, Rosa Damascena Flower Oil, Ceramide AP, Ceramide AS, Ceramide EOP, Ceramide NP, Ceramide NS, Bisabolol, Sodium Hyaluronate, Panthenol, Aloe Barbadensis Leaf, Yucca Brevifolia Root Extract, Abronia Villosa Leaf Extract, Agave Americana Stem Extract, Fouquieria Splendens Stem Extract, Larrea Tridentata Extract, Oenothera Biennis (Evening Primrose) Root Extract, Opuntia Coccinellifera Flower Extract, Theobroma Cacao (Cocoa) Seed Butter, Rosmarinus Officinalis (Rosemary) Leaf Extract, Helianthus Annuus (Sunflower) Seed Oil, Iron Oxides, Cetyl Alcohol, Octyldodecyl Oleate, Ethylhexyl Palmitate, Sodium Gluconate, Coco-Glucoside, Citric Acid, Arachidyl Alcohol, Arachidyl Glucoside, Behenyl Alcohol, Hydrogenated Lecithin, Cellulose Gum, Caprylhydroxamic Acid, Caprylyl Glycol
- Other Information
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
EVERYDAYHUMANS ROSE FROM ABOVE SPF 35 SUNSCREEN BASE
zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72098-006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 157 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) COCONUT OIL (UNII: Q9L0O73W7L) DIHEPTYL SUCCINATE (UNII: 057N7SS26Y) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024) SHEA BUTTER (UNII: K49155WL9Y) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) SQUALANE (UNII: GW89575KF9) GLYCERIN (UNII: PDC6A3C0OX) ROSA X DAMASCENA FLOWER OIL (UNII: 18920M3T13) CERAMIDE AP (UNII: F1X8L2B00J) CERAMIDE NP (UNII: 4370DF050B) CERAMIDE NG (UNII: C04977SRJ5) LEVOMENOL (UNII: 24WE03BX2T) HYALURONATE SODIUM (UNII: YSE9PPT4TH) PANTHENOL (UNII: WV9CM0O67Z) ALOE VERA LEAF (UNII: ZY81Z83H0X) YUCCA BREVIFOLIA ROOT (UNII: KC82I6XYAZ) ABRONIA VILLOSA LEAF (UNII: A138B5260A) AGAVE AMERICANA STEM (UNII: 21BU87042T) FOUQUIERIA SPLENDENS STEM (UNII: 321SWI055M) OENOTHERA BIENNIS ROOT (UNII: SL194W0S0F) OPUNTIA COCHENILLIFERA FLOWER (UNII: A8ZJY40G5N) COCOA BUTTER (UNII: 512OYT1CRR) ROSEMARY (UNII: IJ67X351P9) SUNFLOWER OIL (UNII: 3W1JG795YI) FERRIC OXIDE RED (UNII: 1K09F3G675) CETYL ALCOHOL (UNII: 936JST6JCN) OCTYLDODECYL OLEATE (UNII: MCA43PK7MH) ETHYLHEXYL PALMITATE (UNII: 2865993309) SODIUM GLUCONATE (UNII: R6Q3791S76) COCO GLUCOSIDE (UNII: ICS790225B) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU) ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ) DOCOSANOL (UNII: 9G1OE216XY) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) CAPRYLYL GLYCOL (UNII: 00YIU5438U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72098-006-01 1 in 1 CARTON 04/15/2022 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 04/15/2022 Labeler - EVERYDAY GROUP LIMITED (664624682)
