HERO FORCE SHIELD SUPERBEAM SUNSCREEN SPF 30 APRICOT- zinc oxide lotion 
Church & Dwight Co., 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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Hero Force Shield Superbeam Sunscreen SPF 30 Apricot

Drug Facts

Active ingredient

Zinc Oxide 17.53%

Purpose

Sunscreen

Uses

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 if

  • irritation becomes severe.

Keep out of reach of children.

Directions

Inactive ingredients

water (aqua), caprylic/capric triglyceride, propanediol, C13-15 alkane, C15-19 alkane, butyloctyl salicylate, bis-diglyceryl polyacyladipate-2, octyldodecanol, cetearyl alcohol, polyacrylate crosspolymer-6, hippophae rhamnoides oil, betaine, mica, musa sapientum (banana) leaf/trunk extract, silica, coco-glucoside, arachidyl alcohol, xanthan gum, polyhydroxystearic acid, polyglyceryl-3 polyricinoleate, isostearic acid, lecithin, polyglyceryl-3 lactate/laurate, polyglycerin-3, bisabolol, tocopherol, behenyl alcohol, caprylhydroxamic acid, sodium dilauramidoglutamide lysine, citric acid, arachidyl glucoside, ectoin, niacinamide, maltodextrin, sodium citrate, sodium phytate, terminalia ferdinandiana fruit extract, lactobacillus ferment, tin oxide, glucose, leuconostoc/radish root ferment filtrate, yellow iron oxide, red iron oxide, titanium dioxide

Questions or comments?

347-669-0686

Distributed by Hero Cosmetics, Inc.
New York, NY 10013

PRINCIPAL DISPLAY PANEL - 50 ml Tube Box

Hero.

FORCE SHIELD

Superbeam Sunscreen
Broad Spectrum SPF 30

Protects acne-prone skin from UVA/
UVB with Zinc Oxide. Formulated with
Pearl + Apricot Pigments.

50 ml / 1.69 fl. oz.

PRINCIPAL DISPLAY PANEL - 50 ml Tube Box
HERO FORCE SHIELD SUPERBEAM SUNSCREEN SPF 30 APRICOT 
zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10237-004
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide175.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
PROPANEDIOL (UNII: 5965N8W85T)  
C13-15 ALKANE (UNII: 114P5I43UJ)  
C15-19 ALKANE (UNII: CI87N1IM01)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
BIS-DIGLYCERYL POLYACYLADIPATE-2 (UNII: 6L246LAM9T)  
OCTYLDODECANOL (UNII: 461N1O614Y)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)  
BETAINE (UNII: 3SCV180C9W)  
MICA (UNII: V8A1AW0880)  
BANANA (UNII: 4AJZ4765R9)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
COCO GLUCOSIDE (UNII: ICS790225B)  
ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)  
XANTHAN GUM (UNII: TTV12P4NEE)  
ISOSTEARIC ACID (UNII: X33R8U0062)  
POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)  
LEVOMENOL (UNII: 24WE03BX2T)  
TOCOPHEROL (UNII: R0ZB2556P8)  
DOCOSANOL (UNII: 9G1OE216XY)  
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
SODIUM DILAURAMIDOGLUTAMIDE LYSINE (UNII: MNJ7VPT2R5)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)  
ECTOINE (UNII: 7GXZ3858RY)  
NIACINAMIDE (UNII: 25X51I8RD4)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
PHYTATE SODIUM (UNII: 88496G1ERL)  
KAKADU PLUM (UNII: 0ZQ1D2FDLI)  
STANNIC OXIDE (UNII: KM7N50LOS6)  
ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)  
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColorORANGEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10237-004-001 in 1 BOX07/01/2023
150 mL in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart35207/01/2023
Labeler - Church & Dwight Co., Inc. (001211952)

Revised: 8/2023
Document Id: 420a0687-9abf-4a80-9795-8617708ef487
Set id: 133dc4db-6598-4400-8aa4-022f66eb28fc
Version: 1
Effective Time: 20230825
 
Church & Dwight Co., Inc.