NO SUN FACE SPF 50- zinc oxide, titanium dioxide cream 
Naos USA, Inc.

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.

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NO SUN FACE SPF 50

Drug Facts

Active Ingredients

Zinc Oxide 19.9%

Titanium Dioxide 9%

Purpose

Sunscreen

Uses

Help prevent sunburn.

Warnings

For external use only.

Do not use

on 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 reach of children.

If swallowed, call a poison control centre or get medical help right away.

Directions

  • Adults 18 years and older:
    • Apply liberally and evenly 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. ; and
    • Wear long-sleeve shirts, pants, hats and sunglasses.
    • Children under 6 months of age: ask a doctor.

Other information

  • Keep the product between 15-30ºC (59-86ºF).
  • Protect the product in this container from excessive heat and direct sun.

Inactive Ingredients

Cyclopentasiloxane, Aqua/Water, Cyclohexasiloxane, Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone, Butylene Glycol, Dimethicone, Ethylhexyl Palmitate, Aluminum Hydroxide, Stearic Acid, Peg/Ppg-18/18 Dimethicone, Tocopheryl Acetate Sodium Chloride, Triethoxycaprylylsilane, Creatine, Glycyrrhetinic Acid, Mannitol, Pentylene Glycol, Sodium Dextran Sulfate, Hydrolyzed Soy Protein, Hydrolyzed Wheat Protein, Phenoxyethanol, Propylene Glycol, Caprylyl Glycol, Artemia Extract, Xanthan Gum, Carnosine, Disodium Adenosine Triphosphate, Tocopherol, Laminaria Digitata Extract, Potassium Sorbate. [Es873]

Questions?

Call 1-877-443-3762

Package Labeling:

Outer Label3Inner Label3

NO SUN FACE SPF 50 
zinc oxide, titanium dioxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:14324-012
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION199 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE90 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
WATER (UNII: 059QF0KO0R)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
ETHYLHEXYL PALMITATE (UNII: 2865993309)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
CREATINE (UNII: MU72812GK0)  
ENOXOLONE (UNII: P540XA09DR)  
MANNITOL (UNII: 3OWL53L36A)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
HYDROLYZED SOY PROTEIN (ENZYMATIC; 2000 MW) (UNII: 1394NXB9L6)  
HYDROLYZED WHEAT PROTEIN (ENZYMATIC; 3000 MW) (UNII: J2S07SB0YL)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
XANTHAN GUM (UNII: TTV12P4NEE)  
CARNOSINE (UNII: 8HO6PVN24W)  
ADENOSINE TRIPHOSPHATE DISODIUM (UNII: 5L51B4DR1G)  
TOCOPHEROL (UNII: R0ZB2556P8)  
LAMINARIA DIGITATA (UNII: 15E7C67EE8)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:14324-012-001 in 1 BOX01/31/201809/30/2022
150 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35201/31/201809/30/2022
Labeler - Naos USA, Inc. (080727572)

Revised: 10/2022
 
Naos USA, Inc.