HEB SHIMMER SUNSCREEN SPF 50- avobenzone, homosalate, octisalate, octocrylene lotion 
H.E.B

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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HEB Shimmer Sunscreen SPF 50 Lotion

Active Ingredients

Acobenzone 3.0%, Homosalate 15.0%, Octisalate 5.0%, Octocrylene 7.0%

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 doctor if

• rash occurs

Keep out of reach of children.

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

Directions

• after 80 minutes of swimming or sweating

• immediately after towel drying

• at least every 2 hours

• limit time in the sun, especially from 10am-2pm

• wear long-sleeved shirts, pants, hats, and sunglasses.

Other Information

Inactive Ingredient(s)

water, tridecyl salicylate, sorbitol, stearic acid, triethanolamine, aluminum starch octenylsuccinate, aloe barbadensis leaf juice, polyethyloxazoline, carbomer, dimethicone, tocopherol, polyglyceryl-3 distearate, caprylyl glycol, phenoxyethanol, ethylhexylglycerin, sorbitan isostearate, benzyl alcohol, fragrance, polyethylene terephthalate, polyurethane-33, aluminum powder, red 7, yellow 5, titanium dioxide, iron oxides, mica

Label

HEB58607A1

HEB SHIMMER SUNSCREEN SPF 50 
avobenzone, homosalate, octisalate, octocrylene lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-041
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE150 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE70 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
.ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)  
MICA (UNII: V8A1AW0880)  
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
POLYETHYLOXAZOLINE (5000 MW) (UNII: HNX7574GTX)  
POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV)  
TRIDECYL SALICYLATE (UNII: AZQ08K38Z1)  
POLYETHYLENE TEREPHTHALATE (INTRINSIC VISCOSITY 1.00-2.00) (UNII: KJ6GWA9DJ0)  
ALUMINUM (UNII: CPD4NFA903)  
D&C RED NO. 7 (UNII: ECW0LZ41X8)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
TROLAMINE (UNII: 9O3K93S3TK)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
SORBITOL (UNII: 506T60A25R)  
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37808-041-0989 mL in 1 TUBE; Type 0: Not a Combination Product05/08/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM02005/08/2020
Labeler - H.E.B (007924756)

Revised: 2/2023
Document Id: f5930029-4c97-2576-e053-2995a90a7bed
Set id: f5930029-4c96-2576-e053-2995a90a7bed
Version: 1
Effective Time: 20230225
 
H.E.B