NEUTROGENA HYDRO BOOST CITY SHIELD WATER BROAD SPECTRUM SPF 25- avobenzone, homosalate, octisalate, and octocrylene gel

Neutrogena Hydro Boost City Shield water Broad Spectrum SPF 25 by

Drug Labeling and Warnings

Neutrogena Hydro Boost City Shield water Broad Spectrum SPF 25 by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active Ingredients	Purpose
Avobenzone (2%)	Sunscreen
Homosalate (4%)	Sunscreen
Octisalate (4%)	Sunscreen
Octocrylene (2%)	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

For sunscreen use:

• apply generously and evenly 15 minutes before sun exposure
• reapply at least every 2 hours
• use a water resistant sunscreen if swimming or sweating
• 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, Glycerin, Caprylyl Methicone, Methyl Methacrylate Crosspolymer, Pentylene Glycol, Sodium Acryloyldimethyltaurate/VP Crosspolymer, Phenoxyethanol, Glyceryl Stearate, Chlorphenesin, Tocopheryl Acetate, Sodium Hyaluronate, Disodium EDTA, Ethylhexylglycerin, Fragrance, Sodium Hydroxide, Blue 1, Red 40

Questions?

800-582-4048; Outside US, dial collect 215-273-8755. neutrogena.com

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 48 g Jar Carton

NEW

Hydro Boost

City Shield™

water gel

sunscreen

BROAD SPECTRUM SPF 25

protects against pollution and

replenishes for soft, supple skin

Neutrogena®

NET WT. 1.7 OZ. (48 g)

INGREDIENTS AND APPEARANCE

NEUTROGENA HYDRO BOOST CITY SHIELD WATER BROAD SPECTRUM SPF 25 
avobenzone, homosalate, octisalate, and octocrylene gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0397
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX)	Avobenzone	20 mg  in 1 g
Homosalate (UNII: V06SV4M95S) (Homosalate - UNII:V06SV4M95S)	Homosalate	40 mg  in 1 g
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	40 mg  in 1 g
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	20 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)
Caprylyl Trisiloxane (UNII: Q95M2P1KJL)
Methyl Methacrylate/Glycol Dimethacrylate Crosspolymer (UNII: EG97988M5Q)
Pentylene Glycol (UNII: 50C1307PZG)
Phenoxyethanol (UNII: HIE492ZZ3T)
Glyceryl Monostearate (UNII: 230OU9XXE4)
Chlorphenesin (UNII: I670DAL4SZ)
Hyaluronate Sodium (UNII: YSE9PPT4TH)
Edetate Disodium Anhydrous (UNII: 8NLQ36F6MM)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Ethylhexylglycerin (UNII: 147D247K3P)
Sodium Hydroxide (UNII: 55X04QC32I)
Fd&C Blue No. 1 (UNII: H3R47K3TBD)
Fd&C Red No. 40 (UNII: WZB9127XOA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0397-1	1 in 1 CARTON	10/01/2018
1		48 g in 1 JAR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part352	10/01/2018

Labeler - Johnson & Johnson Consumer Inc. (002347102)