EVERYDAYHUMANS ROSE FROM ABOVE SPF 35 SUNSCREEN BASE- zinc oxide lotion

Everydayhumans Rose from above SPF 35 sunscreen base by

Drug Labeling and Warnings

Everydayhumans Rose from above SPF 35 sunscreen base by is a Otc medication manufactured, distributed, or labeled by EVERYDAY GROUP LIMITED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Zinc Oxide 15.7%

Purpose

Sunscreen

Uses

• Helps prevent sunburn
• If used as directed with other sun protection measures (see ) decreases the risk of skin cancer and early skin aging caused by the sun Directions

Warnings

For external use only

Do not use

on damaged or broken skin 

When using this product

keep out of eyes, rinse with water to remove

Stop use and ask a doctor 

ir rash occurs

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away

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

Protect the product in this container from excessive heat and direct sun. Store below 86°F/30°C. May stain some fabric

Package Labeling:

INGREDIENTS AND APPEARANCE

EVERYDAYHUMANS ROSE FROM ABOVE SPF 35 SUNSCREEN BASE 
zinc oxide lotion

Product 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)