70 DRY TOUCH SPF 70- avobenzone 3% homosalate 15% octisalate 5% octocrylene 10% oxybenzone 3% stick

70 Dry Touch SPF 70 by

Drug Labeling and Warnings

70 Dry Touch SPF 70 by is a Otc medication manufactured, distributed, or labeled by Walgreens, Product Quiest Mfg. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient                                     Purpose
Avobenzone-3%
Homosalate-15%                                      Sunscreen
Octisalate-5%
Octocrylene-10%
Oxybenzone-3%

PURPOSE

INDICATIONS & USAGE

Uses Helps prevent sunburn

WARNINGS

Warnings 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

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

DOSAGE & ADMINISTRATION

Directions

Remove cap and twist up tube.
See important warnings under "When using this
product" apply liberally 15 minutes before sun
exposure 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,

egularly 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

INACTIVE INGREDIENT

Inactive ingredients Adipic Acid/Diglycol Crosspolymer, Beeswax,
BHT, C12-15 Alkyl Benzoate, Caprylyl Glycol,
Fragrance, Neopentyl Glycol Diethylhexanoate,
Neopentyl Glycol Diisostearate, Octyldodecyl
Neopentanoate, Ozokerite, Paraffin, Petrolatum,
Polyester-8, Polyethylene, Silica.

Questions? 1-800-925-4733

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

70 DRY TOUCH SPF 70 
avobenzone 3% homosalate 15% octisalate 5% octocrylene 10% oxybenzone 3% stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-1125
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Avobenzone (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	Avobenzone	3 g  in 100 g
Homosalate (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	Homosalate	15 g  in 100 g
Octisalate (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	Octisalate	5 g  in 100 g
Octocrylene (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	Octocrylene	10 g  in 100 g
Oxybenzone (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	Oxybenzone	3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
YELLOW WAX (UNII: 2ZA36H0S2V)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
Caprylyl Glycol (UNII: 00YIU5438U)
NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C)
Neopentyl Glycol Diisostearate (UNII: 4M6OQ34JWW)
Octyldodecyl Neopentanoate (UNII: X8725R883T)
CERESIN (UNII: Q1LS2UJO3A)
Paraffin (UNII: I9O0E3H2ZE)
Petrolatum (UNII: 4T6H12BN9U)
POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-1125-01	43 g in 1 PACKAGE; Type 0: Not a Combination Product	12/07/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	12/07/2015

Labeler - Walgreens (008965063)

Registrant - Product Quiest Mfg (927768135)

Establishment
Name	Address	ID/FEI	Business Operations
Product Quiest Mfg		927768135	manufacture(0363-1125) , label(0363-1125)