ROC MULTI CORREXION 5 IN 1 CHEST, NECK AND FACE SUNSCREEN BROAD SPECTRUM SPF 30- avobenzone, homosalate, octisalate, and octocrylene cream

RoC Multi Correxion 5 in 1 Chest, Neck and Face by

Drug Labeling and Warnings

RoC Multi Correxion 5 in 1 Chest, Neck and Face 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

Avobenzone 2%
Homosalate 4%
Octisalate 4%
Octocrylene 2%

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

For sunscreen use:

• apply generously 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, Propylene Glycol, Glycerin, Isononyl Isononanoate, Dimethicone, Steareth-2, Ethylhexyl Palmitate, Styrene/Acrylates Copolymer, Butyrospermum Parkii (Shea) Butter, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Hexylresorcinol, Steareth-21, Ammonium Acryloyldimethyltaurate/VP Copolymer, Behenyl Alcohol, Phenoxyethanol, Dimethicone Crosspolymer, Ascorbyl Glucoside, Sclerotium Gum, Chlorphenesin, Fragrance, Disodium EDTA, Tocopheryl Acetate, Maltodextrin, Ethylhexylglycerin, Sodium Hydroxide, Butylene Glycol, Peucedanum Graveolens (Dill) Extract, Rubus Fruticosus (Blackberry) Leaf Extract, Xanthan Gum

Questions?

Call toll-free 800-762-1964 or 215-273-8755 (collect) or visit www.rocskincare.com

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

PRINCIPAL DISPLAY PANEL - 48 g Jar Carton

RoC®
WE KEEP OUR PROMISES®

MULTI CORREXION®
5 IN 1
CHEST, NECK & FACE CREAM

WITH
SUNSCREEN
BROAD SPECTRUM SPF 30

NET WT. 1.7 oz (48 g)

INGREDIENTS AND APPEARANCE

ROC MULTI CORREXION 5 IN 1 CHEST, NECK AND FACE   SUNSCREEN BROAD SPECTRUM SPF 30
avobenzone, homosalate, octisalate, and octocrylene cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0224
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)
Propylene Glycol (UNII: 6DC9Q167V3)
Glycerin (UNII: PDC6A3C0OX)
Isononyl Isononanoate (UNII: S4V5BS6GCX)
Dimethicone (UNII: 92RU3N3Y1O)
Steareth-2 (UNII: V56DFE46J5)
Ethylhexyl Palmitate (UNII: 2865993309)
Shea Butter (UNII: K49155WL9Y)
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR)
Hexylresorcinol (UNII: R9QTB5E82N)
Steareth-21 (UNII: 53J3F32P58)
Ammonium Acryloyldimethyltaurate/VP Copolymer (UNII: W59H9296ZG)
Docosanol (UNII: 9G1OE216XY)
Phenoxyethanol (UNII: HIE492ZZ3T)
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
Ascorbyl Glucoside (UNII: 2V52R0NHXW)
Betasizofiran (UNII: 2X51AD1X3T)
Chlorphenesin (UNII: I670DAL4SZ)
Edetate Disodium Anhydrous (UNII: 8NLQ36F6MM)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Maltodextrin (UNII: 7CVR7L4A2D)
Ethylhexylglycerin (UNII: 147D247K3P)
Sodium Hydroxide (UNII: 55X04QC32I)
Butylene Glycol (UNII: 3XUS85K0RA)
DILL (UNII: Y05PC4JZRH)
Rubus Fruticosus Leaf (UNII: YQ2S06L8S9)
Xanthan Gum (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0224-1	1 in 1 CARTON	09/01/2015
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	09/01/2015

Labeler - Johnson & Johnson Consumer Inc. (002347102)