BABY PURE GENTLE SUNSTICK SPF 60 CVS- titanium dioxide 6.00% zinc oxide 4.70% stick

Baby Pure Gentle SunStick SPF 60 by

Drug Labeling and Warnings

Baby Pure Gentle SunStick SPF 60 by is a Otc medication manufactured, distributed, or labeled by CVS, Product Quest Mfg, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Titanium Dioxide 6.0%

Zinc Oxide 4.7%

PURPOSE

SUnscreen

Uses:

helps prevent sunburn

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.

If product is swallowedm ger medical help or contact a Posion Control Center right away.

Directions:

• 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 Measure. Spending Time in the sun increases your risk of skin cancer and early 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 

Other information

• protect this product from excessive heat and direct sun.

PRINCIPAL DISPLAY PANEL

CVS

pharmacy 

BABY

PURE & GENTLE

SUNSTICK

BROAD SPECTRUM SPF 60

UVA/UVB protection

Sunscreen

Fragrance free

Hypoallergenic, non-irritating

Water resistant (80 minutes)

For ears, nose & face

COMPARE TO NEUTROGENA

PURE & FREE BABY STICK

NET WT 0.47 OZ (13.3 g)

INGREDIENTS AND APPEARANCE

BABY PURE GENTLE SUNSTICK SPF 60  CVS
titanium dioxide 6.00% zinc oxide 4.70% stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59779-270
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	6 g  in 100 g
Zinc Oxide (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	4.7 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
YELLOW WAX (UNII: 2ZA36H0S2V)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
CETYL ALCOHOL (UNII: 936JST6JCN)
DIMETHICONE (UNII: 92RU3N3Y1O)
CANDELILLA WAX (UNII: WL0328HX19)
ISOSTEARIC ACID (UNII: X33R8U0062)
NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C)
CERESIN (UNII: Q1LS2UJO3A)
PARAFFIN (UNII: I9O0E3H2ZE)
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
STEARIC ACID (UNII: 4ELV7Z65AP)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59779-270-01	13.3 g in 1 BOTTLE; Type 0: Not a Combination Product	11/17/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	11/17/2014

Labeler - CVS (062312574)

Registrant - Product Quest Mfg, LLC (927768135)

Establishment
Name	Address	ID/FEI	Business Operations
Product Quest Mfg, LLC		927768135	manufacture(59779-270) , label(59779-270)