SPF 50 Sunscreen Spray 055.000/055AA

Sunscreen by

Drug Labeling and Warnings

Sunscreen by is a Otc medication manufactured, distributed, or labeled by Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SUNSCREEN- avobenzone, homosalate, octisalate, octocrylene spray 
Vi-Jon, LLLC

----------

SPF 50 Sunscreen Spray
055.000/055AA

Active Ingredients

Avobenzone 3%

Homosalate 15%

Octisalate 5%

Octocrylene 8%

Purpose

Sunscreen

Uses

• helps prevent sunburn
• if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Warnings

For external use only

Flammable

Keep away from fire or flame.

• after application, wait until product dries before approacing a souce of heat or flame, or before smoking

Do not use

• on damaged or broken skin

When using this product

• keep out of eyes. Rinse with water to remove.  contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120ºF.

Stop use and ask a doctor if

• rash occurs

keep out of reach of children

if swallowed, get medical help or contact a Poison Conrol Center right away

Direction

■ spray liberally and spread evenly by hand 15 minutes before sun exposure
■ apply to all skin exposed to the sun
■ hold container 4 to 6 inches from the skin to apply
■ do not spray directly into face. Spray on hands then apply to face.
■ do not apply in windy conditions
■ use in a well-ventilated area and avoid inhalation
■ reapply:
■ after 80 minutes of swimming or sweating
■ immediately after towel drying
■ at least every 2 hours
■ Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
■ limit time in the sun, especially from 10 a.m.–2 p.m.
■ wear long-sleeved shirts, pants, hats and sunglasses
■ children under 6 months of age: Ask a doctor

Other information

• protect the product in the container from excessive heat and direct sun

Inactive ingredients

alcohol denat., acrylates/octylacrylamide copolymer, glycerin, triethanolamine, tocopherol, butyloctyl salicylate, fragrance

May stain or damage some fabrics of surfaces

Oxybenzone & Octinoxate free

This product is not manufactured or distributed by S.C. Johnson & Sons, Inc., distributor of Sun Burn Premium Moisturizing Sunscreen Spray Broad Spectrum SPF 50.

DISTRUBUTED BY DOLGENCORP, LLC

100 MISSION RIDGE

GOODLETTSVILLE, TN 37072

100% Satisfaction Guaranteed! (888)309-9030

Principal Display Panel

Wild

Tropics

SUNSCREEN

SPRAY

BROAD SPECTRUM SPF 50

OCTINOXAQTE & OXYBENZONE FREE

HYPOALLERGENIC

DERMATP;PGOST TESTED

WATER RESISTANT (80 MINUTES)

FRESH BANANA SCENT

Compare to Sun Bum Premium

Moiturizing Sunscreen Spray

SPF

50

NET WT 5.5 OZ (156 g)

SUNSCREEN 
avobenzone, homosalate, octisalate, octocrylene spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0869-0055
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	150 mg  in 1 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	50 mg  in 1 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	80 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
STEAROXYTRIMETHYLSILANE (UNII: 9862TW94B2)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
TOCOPHEROL (UNII: R0ZB2556P8)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0869-0055-14	156 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/19/2022	03/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	09/19/2022	03/01/2024

Labeler - Vi-Jon, LLLC (088520668)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(0869-0055)

Revised: 3/2024

Document Id: 147ff593-8aa9-8eeb-e063-6394a90a7781

34390-5

Set id: ee3a23b3-189a-43de-b638-cecc0993e3f2

Version: 2

Effective Time: 20240325

 <