NEUTROGENA ULTRA SHEER DRY TOUCH SUNSCREEN BROAD SPECTRUM SPF 30- avobenzone, homosalate, octisalate, and octocrylene lotion

Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 30 by

Drug Labeling and Warnings

Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 30 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 INGREDIENT

Active ingredients	Purpose
Avobenzone 2.5%	Sunscreen
Homosalate 6%	Sunscreen
Octisalate 4.5%	Sunscreen
Octocrylene 8%	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.
• keep away from face to avoid breathing it

• 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

• Danger: Flammable. Contents under pressure. Do not use near fire, heat or while smoking. Do not puncture or incinerate. Store at temperature below 120°F (48°C). Use only as directed. Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.

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, Silica, Caprylyl Methicone, Diisopropyl Adipate, Dimethicone, Potassium Cetyl Phosphate, Benzyl Alcohol, Beeswax, Glyceryl Stearate, PEG-100 Stearate, Cetyl Dimethicone, Caprylyl Glycol, Ethylhexylglycerin, Behenyl Alcohol, Sodium Polyacrylate, Acrylates/Dimethicone Crosspolymer, Xanthan Gum, Chlorphenesin, Dimethicone/PEG-10/15 Crosspolymer, Ethylhexyl Stearate, Hydrolyzed Jojoba Esters, Fragrance, Disodium EDTA, Tocopheryl Acetate, BHT, Trideceth-6, Jojoba Esters

Questions?

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®

#1 DERMATOLOGIST RECOMMENDED BRAND

Ultra Sheer®
dry-touch
sunscreen
BROAD SPECTRUM SPF 30

30

helioplex®
broad spectrum uvauvb

lightweight clean feel

oxybenzone free

water resistant (80 minutes)

5.0 FL OZ (147 mL)

INGREDIENTS AND APPEARANCE

NEUTROGENA ULTRA SHEER DRY TOUCH SUNSCREEN BROAD SPECTRUM SPF 30 
avobenzone, homosalate, octisalate, and octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0552
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX)	Avobenzone	25 mg  in 1 mL
Homosalate (UNII: V06SV4M95S) (Homosalate - UNII:V06SV4M95S)	Homosalate	60 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	45 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	80 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Silicon Dioxide (UNII: ETJ7Z6XBU4)
Caprylyl Trisiloxane (UNII: Q95M2P1KJL)
Diisopropyl Adipate (UNII: P7E6YFV72X)
Dimethicone (UNII: 92RU3N3Y1O)
Potassium Cetyl Phosphate (UNII: 03KCY6P7UT)
Benzyl Alcohol (UNII: LKG8494WBH)
Yellow Wax (UNII: 2ZA36H0S2V)
Glyceryl Monostearate (UNII: 230OU9XXE4)
PEG-100 Stearate (UNII: YD01N1999R)
Caprylyl Glycol (UNII: 00YIU5438U)
Ethylhexylglycerin (UNII: 147D247K3P)
Docosanol (UNII: 9G1OE216XY)
Xanthan Gum (UNII: TTV12P4NEE)
Chlorphenesin (UNII: I670DAL4SZ)
Ethylhexyl Stearate (UNII: EG3PA2K3K5)
Hydrolyzed Jojoba Esters (Acid Form) (UNII: UDR641JW8W)
Edetate Disodium Anhydrous (UNII: 8NLQ36F6MM)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Butylated Hydroxytoluene (UNII: 1P9D0Z171K)
Trideceth-6 (UNII: 3T5PCR2H0C)
JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL)
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
CETYL DIMETHICONE 150 (UNII: 5L694Y0T22)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0552-5	147 mL in 1 TUBE; Type 0: Not a Combination Product	10/07/2019
2	NDC: 69968-0552-3	88 mL in 1 TUBE; Type 0: Not a Combination Product	10/07/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	10/07/2019

Labeler - Johnson & Johnson Consumer Inc. (002347102)