EXCHANGE SELECT SUNSCREEN SPF 45- octinoxate oxybenzone lotion

Exchange Select Sunscreen by

Drug Labeling and Warnings

Exchange Select Sunscreen by is a Otc medication manufactured, distributed, or labeled by ARMY AND AIR FORCE EXCHANGE SERVICE. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Avobenzone 2.0%
Homosalate 12.0%
Octisalate 5.0%
Octtocrylene 1.6%
Oxybenzone 3.5%

Purpose

Sunscreen

Uses

• helps prevent sunburn
• higher SPF gives more sunburn protection
• retains SPF after 80 minutes of activity in the water
  

Warnings

For external use only

When using this product

• keep out of eyes. Rinse with water to remove.
  

Stop use and ask a doctor if

• rash or irritation develops and lasts.
  

Keep Out of the reach of children.

If swallowed get medical help or contact a Poison Control Center right away.

Directions

• apply generously before sun exposure and as needed
• children under 6 months of age:ask a doctor
• reapply frequently and after towel drying, swimming or perspiring.
  

Other Information

• May stain some fabrics
  
• Sun Alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risks of skin aging, skin cance, and other harmful effects of the sun.
  

Inactive ingredients

Water, Sorbitan Isostearate, Sorbitol, Triethanolamine, Octadecene/MA Copolymer, Polyglyceryl-3 Distearate, VP/Eicosene Copolymer, Benzyl Alcohol, Barium Sulfate, Dimethicone, Stearic Acid, Carbomer, Phenethyl Alcohol, Simmondsia Chinensis (Jojoba) Seed Oil, Tocopherol, Disodium EDTA, Aloe Barbadensis Leaf Juice Powder, Methylparaben, Propylparaben.

Principal Display Panel

exchange
select
X
SUNSCREEN
Broad Spectrum Lotion
SPF
45
UVA/UVB Protection
Very Water Resistant
4 FL. OZ. (118 mL)

INGREDIENTS AND APPEARANCE

EXCHANGE SELECT SUNSCREEN  SPF 45
octinoxate oxybenzone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55301-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	2 g  in 100 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	12 g  in 100 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	1.6 g  in 100 g
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	3.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
STEARIC ACID (UNII: 4ELV7Z65AP)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
SORBITOL (UNII: 506T60A25R)
BARIUM SULFATE (UNII: 25BB7EKE2E)
POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
TROLAMINE (UNII: 9O3K93S3TK)
BENZYL ALCOHOL (UNII: LKG8494WBH)
DIMETHICONE (UNII: 92RU3N3Y1O)
JOJOBA OIL (UNII: 724GKU717M)
TOCOPHEROL (UNII: R0ZB2556P8)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
DIMETHICONE (UNII: 92RU3N3Y1O)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55301-001-13	113 g in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	11/15/2012

Labeler - ARMY AND AIR FORCE EXCHANGE SERVICE (001695568)