NEUTROGENA SHEER ZINC DRY-TOUCH SUNSCREEN BROAD SPECTRUM SPF50- zinc oxide lotion

Neutrogena Sheer Zinc DRY-TOUCH by

Drug Labeling and Warnings

Neutrogena Sheer Zinc DRY-TOUCH by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active ingredients

Zinc Oxide 21.6%

Purpose

Sunscreen

Uses

• 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

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 swallowed, get medical help or contact a Poison 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 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 value 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-sleeved shirts, pants, hats, and sunglasses
• children under 6 months of age: Ask a doctor

Other information

• protect this product from excessive heat and direct sun
• may stain some fabrics

Inactive ingredients

• Water, C 12-15 Alkyl Benzoate, Octyldodecyl Citrate Crosspolymer, Styrene/Acrylates Copolymer, Phenyl Trimethicone, Cetyl PEG/PPG-10/1 Dimethicone, Dimethicone, Polyhydroxystearic Acid, Glycerin, Ethyl Methicone, Cetyl Dimethicone, Triethoxycaprylylsilane, Silica, Colloidal Oatmeal, Tocopheryl Acetate, Chrysanthemum Parthenium (Feverfew) Flower/Leaf/Stem Juice, Glyceryl Behenate, Phenethyl Alcohol, Caprylyl Glycol, Cetyl Dimethicone/Bis-Vinyldimethicone Crosspolymer, Acrylates/Dimethicone Copolymer, Sodium Chloride

Questions or Comments?

Call toll-free 800-299-4786 or 215-273-8755 (collect).

www.neutrogena.com

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Distributed by: JOHNSON & JOHNSON CONSUMER INC. Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 147 mL Tube Label

VALUE SIZE
Neutrogena

Sheer Zinc ®
DRY-TOUCH
SUNSCREEN

Broad Spectrum SPF 50
50

pureSCREEN®
100% zinc oxide uva uvb

ACCEPTED
e
NATIONALECZEMA.ORG

NATIONAL
ECZEMA
ASSOCIATION

hypoallergenic
water resistant
(80 minutes)

#1 DERMATOLOGIST
RECOMMENDED SUNCARE

5.0 FL OZ (147 mL)

INGREDIENTS AND APPEARANCE

NEUTROGENA SHEER ZINC DRY-TOUCH   SUNSCREEN BROAD SPECTRUM SPF50
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0476
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z)	Zinc Oxide	216 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)
OCTYLDODECYL CITRATE CROSSPOLYMER (UNII: X323T6QO4M)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)
Dimethicone (UNII: 92RU3N3Y1O)
Phenyl Trimethicone (UNII: DR0K5NOJ4R)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
Glycerin (UNII: PDC6A3C0OX)
Silicon Dioxide (UNII: ETJ7Z6XBU4)
CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
Feverfew (UNII: Z64FK7P217)
Glyceryl Dibehenate (UNII: R8WTH25YS2)
Caprylyl Glycol (UNII: 00YIU5438U)
Ethyl Methicone (8 Mpa.S) (UNII: 3YWG8XYT8H)
Sodium Chloride (UNII: 451W47IQ8X)
Phenoxyethanol (UNII: HIE492ZZ3T)
CETYL DIMETHICONE/BIS-VINYLDIMETHICONE CROSSPOLYMER (UNII: AE7QA6TW0Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0476-5	147 mL in 1 TUBE; Type 0: Not a Combination Product	12/01/2018
2	NDC: 69968-0476-1	14 mL in 1 TUBE; Type 0: Not a Combination Product	10/17/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part352	10/17/2016

Labeler - Johnson & Johnson Consumer Inc. (002347102)