H.E.B SOLUTIONS SUNSCREEN- ultra spf 100 continuous spray aerosol, spray 
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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H.E.B Solutions Sunscreen Ultra SPF 100 Continuous Spray

Active ingredients

Avobenzone 3.0%, Homosalate 15.0%, Octisalate 5.0%, Octocrylene 10.0%, Oxybenzone 6.0%

Purpose

Sunscreen

Uses

Warnings

For external use only

FLAMMABLE:

   • do not use near heat, flame or while smoking

   • avoid long term storage above 104°F (40°C)

Do not use • on damaged or broken skin.

When using this product • keep out of eyes. Rinse with water to remove. • do not puncture or incinerate. Contents under pressure. • do not store at temperatures above 120°F.

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

   • after 80 minutes of swimming or sweating

   • immediately after towel drying

   • at least every 2 hours

   • limit time in the sun, especially from 10 a.m. - 2 p.m.

   • wear long-sleeve shirts, pants, hats, and sunglasses

Other information

Inactive ingredients

SD alcohol 40-B, butyloctyl salicylate, butylated PVP, polyester-10, propylene glycol dibenzoate, glycerin, caprylic/capric triglyceride, tocopherol, aloe barbadensis leaf juice, saccharomyces/podophyllum peltatum ferment filtrate, chamomilla recutita (matricaria) flower extract, camellia sinensis leaf extract (green tea), fragrance, propylene glycol, butylene glycol

Questions or Comments?

Call toll free 1-800-527-7731

H.E.B Solutions Sunscreen Ultra SPF 100 Continuous Spray

5.5 OZ (156g)

NDC 37808-982-37

Label

H.E.B  SOLUTIONS SUNSCREEN
ultra spf 100 continuous spray aerosol, spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-982
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE150 mg  in 1 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE100 mg  in 1 g
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE60 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
TOCOPHEROL (UNII: R0ZB2556P8)  
GLYCERIN (UNII: PDC6A3C0OX)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
POLYESTER-10 (UNII: 212N9O2MMZ)  
PROPYLENE GLYCOL DIBENZOATE (UNII: EQY32Z1AN4)  
CHAMOMILE (UNII: FGL3685T2X)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37808-982-37156 g in 1 CAN; Type 0: Not a Combination Product01/20/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35201/20/2012
Labeler - H.E.B (007924756)
Registrant - Fruit of the Earth, Inc. (079559467)
Establishment
NameAddressID/FEIBusiness Operations
Fruit of the Earth, Inc.008193513manufacture(37808-982)

Revised: 3/2020
Document Id: cba3d484-8d90-49cd-8567-12924ba102bf
Set id: be80244d-da6d-4d37-b228-4d3fac335caf
Version: 1
Effective Time: 20200310
 
H.E.B