EVERYDAY SUN DEFENSE- zinc oxide cream 
Hommerejuvenate, Inc.

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Active Ingredient

Zinc Oxide 9.4%

Inactive Ingredient

Ammonium Acryloyldimethyltaurate/VP Copolymer, Argania Spinosa Kernel Oil, Bisabolol, Butyrospermum Parkii (Shea Butter) Extract, C12-15 Alkyl Benzoate, C12-20 Glucoside, C14-22 Alcohol, Caprylyl/Capryl Glucoside, Cetearyl Alcohol, Coco Glucoside, Dimethicone, Ethyl Ferulate, Ethylhexylglycerin, Ethylhexylglycerin, Glycerin, Hydroxyethyl Acrylate, Phenoxyethanol, Phospholipids, Polyester-5, Propylene Glycol, Sodium Acryloyl Dimethyl Taurate Copolymer, Sorbitan Oleate Decylglucoside Crosspolymer, Squalane, Tocopheryl Acetate, Triethoxycaprylylsi-lane, Urea, Water

OTC-Ask Doctor


Ask a doctor if rash occurs

OTC-Do Not Use

Do not use on damaged or broken skin

OTC-Keep Out of Reach of Children

Keep out of reach of children. If swallowed, get medical help or contact Poison Control right away

OTC-Purpose

Sunscreen

OTC-Questions

+1) 866-322-3010

OTC-Stop Use

Stop use if rash occurs

OTC-When using

When using this product keep out of eyes
Rinse with water to remove

Indications & Usage Section

High protection against sunburn

- 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 if rash occurs
- Keep out of reach of children. If swallowed, get medical help or contact a Poison Control right away

- Apply generously 15 minutes before sun exposure

- Reapply every 2 hours
- Use a water-resistant sunscreen if swimming or sweating

Everyday Sun Defense

EVERYDAY SUN DEFENSE 
zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83580-010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE9.4 g  in 9.4 g
Inactive Ingredients
Ingredient NameStrength
ARGAN OIL (UNII: 4V59G5UW9X)  
ETHYL FERULATE (UNII: 5B8915UELW)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
SQUALANE (UNII: GW89575KF9)  
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
WATER (UNII: 059QF0KO0R)  
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
COCO GLUCOSIDE (UNII: ICS790225B)  
C14-22 ALCOHOLS (UNII: B1K89384RJ)  
C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
OMEGA-3 FATTY ACIDS (UNII: 71M78END5S)  
GLUCONOLACTONE (UNII: WQ29KQ9POT)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SHEA BUTTER (UNII: K49155WL9Y)  
UREA (UNII: 8W8T17847W)  
SORBIC ACID (UNII: X045WJ989B)  
POLYESTER-5 (TG-38) (UNII: 2L9351NW8W)  
LEVOMENOL (UNII: 24WE03BX2T)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83580-010-0160 g in 1 TUBE; Type 0: Not a Combination Product04/01/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02004/01/2024
Labeler - Hommerejuvenate, Inc. (080651103)
Registrant - Hommerejuvenate, Inc. (080651103)
Establishment
NameAddressID/FEIBusiness Operations
DERMACEUTICAL LABORATORIES LIMITED LIABILITY COMPANY078457159manufacture(83580-010)

Revised: 1/2024
Document Id: 0e7691d1-1c4d-8021-e063-6394a90adec2
Set id: 05aa1a1a-9e4f-2781-e063-6394a90aef6b
Version: 3
Effective Time: 20240108
 
Hommerejuvenate, Inc.