HEB SOLUTIONS SUNSCREEN ULTRA 30- avobenzone, homosalate, octisalate, octocrylene, oxybenzone 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.

----------

HEB Solutions Sunscreen Ultra 30 Lotion

Active ingredients

Avobenzone 2%, Homosalate 7%, Octisalate 5%, Octocrylene 3%, Oxybenzone 4%

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 • rash occurs.

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

Directions

Other information

Inactive ingredients

water, propylene glycol, silica, aluminum starch octenylsuccinate, behenyl alcohol, glyceryl stearate, microcrystalline cellulose, benzyl alcohol, palmitic acid, myristyl alcohol, stearic acid, saccharomyces/podophyllum peltatum ferment filtrate, lauryl alcohol, cetyl alcohol, aloe barbadensis leaf juice, chamomilla recutita (matricaria) flower extract, tocopherol (vitamin E), lecithin, cellulose gum, chlorphenesin, butylated PVP, disodium EDTA, butylene glycol

HEB Solutions Sunscreen Ultra 30 Lotion

8 FL OZ (237)

NDC 37808-941-12

HEB89892A5

HEB SOLUTIONS  SUNSCREEN ULTRA 30
avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-941
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE70 mg  in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE40 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE20 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE30 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
DOCOSANOL (UNII: 9G1OE216XY)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
MYRISTYL ALCOHOL (UNII: V42034O9PU)  
LAURYL ALCOHOL (UNII: 178A96NLP2)  
PALMITIC ACID (UNII: 2V16EO95H1)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
WATER (UNII: 059QF0KO0R)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
TOCOPHEROL (UNII: R0ZB2556P8)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
CHAMOMILE (UNII: FGL3685T2X)  
N-VINYLPYRROLIDINONE (UNII: 76H9G81541)  
YEAST (UNII: 3NY3SM6B8U)  
PODOPHYLLUM (UNII: 2S713A4VP3)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37808-941-12237 mL in 1 TUBE; Type 0: Not a Combination Product02/06/2013
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35202/06/2013
Labeler - H-E-B (007924756)

Revised: 10/2022
Document Id: ea2debcb-891e-339f-e053-2a95a90a4b18
Set id: 947fd351-f902-7111-e053-2995a90a5190
Version: 6
Effective Time: 20221003
 
H-E-B