Hampton Sun SPF 50 Sunscreen Spry

Hampton Sun SPF 50 by

Drug Labeling and Warnings

Hampton Sun SPF 50 by is a Otc medication manufactured, distributed, or labeled by Inspec Solutions. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAMPTON SUN SPF 50- avobenzone, humosalate, octisalate, octocrylene spray 
Inspec Solutions

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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Hampton Sun SPF 50 Sunscreen Spry

Active ingredient

Avobenzone 3.0%

Homosalate 15%

Octisalate 5%

Octocrylene 10%

When using this product:

keep out of eyes. Rinse with water to remove.

Keep away from face to avoid breathing it.

Do not puncture or incinerate, Contents under pressure

Do not store at temperature above 120⁰F

Stop use and ask a doctor if rash occurs.

Avobenzone 3.0% ……………………………………………………………………………… Sunscreen

Homosalate 15.0% ……………………………………………………………………………. Sunscreen

Octisalate 5.0% …………………………………………………………………………………. Sunscreen

Octocrylene 10.0% ……………………………………………………………………………. Sunscreen

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.

Behenyl Alcohol

BHT

Butyloctyl Salicylate

Caprylyl Methicone Dimethicone

Dimethyl Capramide

Disodium EDTA

Ethylhexyl Stearate

Ethylhexylglycerin

Fragrance

Glyceryl Stearate Hydrated Silica

PEG-100 Stearate

Phenoxyethanol

Polyester-8

Sodium Polyacrylate

Styrene/Acrylates Copolymer

Trideceth-6

Trimethylsiloxysilicate

VP/Hexadecene Copolymer

Water

Xanthan Gum

keep out of eyes. Rinse with water to remove.

Keep away from face to avoid breathing it.

Do not puncture or incinerate, Contents under pressure

Do not store at temperature above 120⁰F

Stop use and ask a doctor if rash occurs.

Hampton Sun SPF 50 Sunscreen

HAMPTON SUN SPF 50 
avobenzone, humosalate, octisalate, octocrylene spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 72667-030
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE15 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE10 g  in 100 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
BEHENYL BEHENATE (UNII: K8NU647RJ0)  
DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)  
GLYCERIN (UNII: PDC6A3C0OX)  
TOCOPHEROL (UNII: R0ZB2556P8)  
STEAROXYTRIMETHYLSILANE (UNII: 9862TW94B2)  
ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (75000 MW) (UNII: JU3XHR8VWK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 72667-030-01150 mL in 1 CAN; Type 0: Not a Combination Product06/25/2022
2NDC: 72667-030-0230 mL in 1 CAN; Type 0: Not a Combination Product06/25/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35206/25/2022
Labeler - Inspec Solutions (081030372)
Establishment
NameAddressID/FEIBusiness Operations
Inspec Solutions081030372manufacture(72667-030)

Revised: 6/2022
 

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