JERGENS NATURAL GLOW FACE DAILY MOISTURIZER FOR MEDIUM/TAN SKIN- avobenzone,octisalate, octocrylene lotion

Jergens Natural Glow Face by

Drug Labeling and Warnings

Jergens Natural Glow Face by is a Otc medication manufactured, distributed, or labeled by Kao USA Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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How to Use to get Natural-Looking Color: For best results, use daily as your facial moisturizer. Apply a generous amount evenly over freshly cleansed face, blending into jawline & hairline and avoiding eyebrows. Allow several minutes for it to fully absorb. Wash your hands after application. You will begin to see development of color within several days with no sunless tanner odor. If color change is not as noticeable as desired, apply more frequently.

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Drug Facts

ACTIVE INGREDIENT

Active ingredients

Avobenzone 1.25%

Octisalate 5%

Octocrylene 1.1%

PURPOSE

Purpose

Sunscreen

INDICATIONS & USAGE

Use

helps prevent sunburn

WARNINGS

Warnings

For external use only

DO NOT USE

Do not use on damaged or broken skin

WHEN USING

When using this product keep out of eyes. Rinse with water to remove.

STOP USE

Stop use and ask a doctor if rash occurs

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions
For sunscreen use:

• apply generously and evenly to freshly cleansed face, avoiding eyebrows, 15 minutes before sun exposure
• wash hands after application
• reapply at least every 2 hours*
• use a water resistant sunscreen if swimming or sweating
• children under 6 months of age: Ask a doctor
• 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

STORAGE AND HANDLING

Other information

protect the product in this container from excessive heat and direct sun

INACTIVE INGREDIENT

Inactive ingredients

water, dihydroxyacetone, glycerin, dicaprylyl ether, aluminum starch octenylsuccinate, glyceryl stearate, polyacrylamide, C12-15 alkyl benzoate, phenyl trimethicone, behenyl alcohol, dimethicone, methylparaben, PEG-100 stearate, C13-14 isoparaffin, diethylhexyl 2,6 naphthalate, steareth-2, cetyl alcohol, ethylparaben, fragrance, propylparaben, xanthan gum, laureth-7, citric acid, zea mays (corn) starch,tocopheryl acetate, erythrulose, caramel

QUESTIONS

Questions or comments? 1-800-742-8798

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*If reapplying at least every 2 hours for sunscreen use, a non-glow sunscreen is recommended if color change becomes too intense.

Visit www.jergens.com. Reg. U.S. Pat. & Tm. Off.

Distributed by Kao USA Inc., Cincinnati, OH 45214

©2014 Made in USA

PRINCIPAL DISPLAY PANEL

AWARD WINNING COLOR

GREAT SCENT

JERGENS®

NATURAL GLOW

GRADUALLY CREATES FLAWLESS, NATURAL-LOOKING COLOR WHEN USED ONCE DAILY

FACE

DAILY MOISTURIZER WITH SUNSCREEN

BROAD SPECTRUM SPF 20

OIL FREE

MEDIUM TO TAN SKIN TONES

2 FL OZ (59 mL)

INGREDIENTS AND APPEARANCE

JERGENS NATURAL GLOW FACE  DAILY MOISTURIZER FOR MEDIUM/TAN SKIN
avobenzone,octisalate, octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10596-715
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	0.74 g  in 59 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	2.95 g  in 59 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	0.65 g  in 59 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
STARCH, CORN (UNII: O8232NY3SJ)
DIHYDROXYACETONE (UNII: O10DDW6JOO)
CETYL ALCOHOL (UNII: 936JST6JCN)
DICAPRYLYL ETHER (UNII: 77JZM5516Z)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
DOCOSANOL (UNII: 9G1OE216XY)
DIMETHICONE (UNII: 92RU3N3Y1O)
METHYLPARABEN (UNII: A2I8C7HI9T)
PEG-100 STEARATE (UNII: YD01N1999R)
DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)
STEARETH-2 (UNII: V56DFE46J5)
POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
ETHYLPARABEN (UNII: 14255EXE39)
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
XANTHAN GUM (UNII: TTV12P4NEE)
LAURETH-7 (UNII: Z95S6G8201)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
L-ERYTHRULOSE (UNII: WKK1W5B83O)
CARAMEL (UNII: T9D99G2B1R)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10596-715-20	1 in 1 BOX	02/23/2015
1		59 mL in 1 TUBE; 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	02/23/2015

Labeler - Kao USA Inc. (004251617)