Active Ingredients

Avobenzone 3%

Homosalate 15%

Octisalate 5%

Octocrylene 10%

Oxybenzone 6%

Purpose

Sunscreen

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

For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes. Risne with water to remove.

Keep away from face to avoid breathing it. Contents under pressure-do not puncture or incinerate. Do not store at temperatures above 120ºF.

Stop use and ask a doctor if rash occurs

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

Flammable Do not use near heat, flame or while smoking.

Spray liberally and spread evenly by hand 15 minutes before sun exposure.
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 well ventilated areas.
Reapply:
after 80 minutes of swimming and 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 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-sleeve shirts, pants, hats, and sunglasses.
Children under 6 months: Ask a doctor.

Caprylic/Capric Triglyceride, Diethylhexyl Syringylidene-malonate, Fragrance, SD Alcohol 40-B, VA/Butyl Maleate/Isobornyl Acrylate Copolymer

Call toll free 1-800-840-5225

Principal Display Label

PANAMA JACK BROAD SPECTRUM SPF 100 SUNSCREEN
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone spray

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	26.28 mg in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	131.4 mg in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	43.8 mg in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	87.6 mg in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	52.56 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
ALCOHOL (UNII: 3K9958V90M)
VINYL ACETATE (UNII: L9MK238N77)
MONOBUTYL MALEATE (UNII: F2LD7FVO1L)
ISOBORNYL ACRYLATE (UNII: IX0PRH184P)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:13630-0124-4	177 mL in 1 CAN; Type 0: Not a Combination Product	01/24/2018

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	01/24/2018

Labeler - Prime Packaging Inc. (805987059)

Registrant - Prime Packaging Inc. (805987059)

Name	Address	ID/FEI	Business Operations
Establishment
Prime Enterprises Inc		101946028	manufacture(13630-0124) , analysis(13630-0124)

Name	Address	ID/FEI	Business Operations
Establishment
Prime Packaging Inc.		805987059	label(13630-0124) , pack(13630-0124)