Active Ingredients

Octyl Methoxycinnamate 7%

Titanium Dioxide 2.8%

Purpose

Sunscreen

Use

helps prevent sunburn

Warnings

Skin Cancer/Early Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to prevent sunburn, not skin cancer or early skin aging.

For external use only.

Do not use

on damaged or broken skin

When using this product

Keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor

if rash occurs

Keep out of reach of children.

If product is swallowed, get medical help or call a Poison Control Center right away.

Directions

apply liberally 15 minutes before sun exposure
reapply:
- after 40 minutes of swimming or sweating
- immediately after towel drying
- at least every 2 hours
children under 6 months: Ask a doctor

Other information

protect this product from excessive heat and direct sun
may stain fabrics
for Lot and Expiration Date, see crimp of tube

Inactive Ingredients

Water, Glycerin, Glyceryl Stearate,

PEG-100 Stearate, Stearic acid, Cetearyl Alcohol, Phenoxyethanol,

Acrylates/C10-30 alkyl acrylate crosspolymer, Chlorphenesin,

Triethanolamine, Lavandula Angustifolia (Lavender) Extract,

Salvia Sclarea (Clary) Extract, Hyacinthus Orientalis Extract,

Chamomilla Recutita (Matricaria) Flower/Leaf Extract, Borago

officinalis Extract, Centaurea cyanus flower Extract, Dimethicone,

Butylene Glycol, 1,2-Hexanediol, Ethylhexylglycerin, Disodium

EDTA, Fragrance

Package label

Pure Aid Kids Sunscreen Lotion

tube

KIDS SUNSCREEN
octinoxate and titanium dioxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:67510-0082
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	7 g in 100 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.8 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
PEG-100 STEARATE (UNII: YD01N1999R)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
STEARIC ACID (UNII: 4ELV7Z65AP)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
CHLORPHENESIN (UNII: I670DAL4SZ)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CETYL ALCOHOL (UNII: 936JST6JCN)
DIMETHICONE (UNII: 92RU3N3Y1O)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:67510-0082-5	100 mL in 1 TUBE; Type 0: Not a Combination Product	12/01/2011

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	12/01/2011

Labeler - Kareway Product, Inc. (121840057)

Drug Facts