ANEW CLINICAL ABSOLUTE EVEN SPOT CORRECTING HAND- octinoxate, oxybenzone, avobenzone cream

Anew Clinical by

Drug Labeling and Warnings

Anew Clinical by is a Otc medication manufactured, distributed, or labeled by New Avon LLC, Avon Products, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredientsOCTINOXATE 7.5%, OXYBENZONE 4.0%,
AVOBENZONE 2.0%.......................

Purpose
................................Sunscreen

INDICATIONS & USAGE

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

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.

DOSAGE & ADMINISTRATION

Directions

apply liberally 15 minutes before sun exposure
children under 6 months of age: ask a doctor
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

STORAGE AND HANDLING

Other information

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

INACTIVE INGREDIENT

Inactive ingredients WATER/EAU, GLYCERIN, PENTAERYTHRITYL TETRAETHYLHEXANOATE, STEARETH-2, GLYCOLIC ACID, BEHENYL ALCOHOL, DIMETHICONE, PEG-40 STEARATE, MYRISTYL MYRISTATE, TRISILOXANE, LAURYL LACTATE, ASPARTIC ACID, ZEA MAYS (CORN) KERNEL EXTRACT, PHYTOL, BUTYROSPERMUM PARKII (SHEA) BUTTER, COLA NITIDA SEED EXTRACT, GLYCINE SOJA (SOYBEAN) SEED EXTRACT, PUNICA GRANATUM FRUIT JUICE, RETINYL PALMITATE, DAUCUS CAROTA SATIVA (CARROT) ROOT EXTRACT, ASCORBYL PALMITATE, HELIANTHUS ANNUUS (SUNFLOWER) SEED EXTRACT, RETINOL, GLYCINE SOJA (SOYBEAN) OIL, SAXIFRAGA SARMENTOSA EXTRACT, VITIS VINIFERA (GRAPE) FRUIT EXTRACT, TOCOPHEROL, BETA-CAROTENE, MORUS NIGRA ROOT EXTRACT, SCUTELLARIA BAICALENSIS ROOT EXTRACT, GLYCERYL STEARATE, PEG-100 STEARATE, PVM/MA DECADIENE CROSSPOLYMER, XANTHAN GUM, SILICA, ACRYLATES/CARBAMATE COPOLYMER, MALTODEXTRIN, LECITHIN, TRIMETHYLSILOXYSILICATE, BUTYLENE GLYCOL, AMMONIUM HYDROXIDE, PHENOXYETHANOL, METHYLPARABEN, DISODIUM EDTA, BHT, PARFUM/FRAGRANCE.

QUESTIONS

Questions? 1-800-FOR-AVON

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANEW CLINICAL  ABSOLUTE EVEN SPOT CORRECTING HAND
octinoxate, oxybenzone, avobenzone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10096-0290
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
octinoxate (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	octinoxate	75 mg  in 1 g
oxybenzone (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	oxybenzone	40 mg  in 1 g
avobenzone (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	avobenzone	20 mg  in 1 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10096-0290-2	1 in 1 CARTON
1	NDC: 10096-0290-1	75 g 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	11/11/2012

Labeler - New Avon LLC (080143520)

Establishment
Name	Address	ID/FEI	Business Operations
Avon Products, Inc		005149471	manufacture(10096-0290)