PATRICIA WEXLER SKIN BRIGHTENING DAILY MOISTURIZER WITH SUNSCREEN BROAD SPECTRUM SPF 28- avobenzone, octinoxate, octisalate, oxybenzone lotion

Patricia Wexler Skin Brightening Daily Moisturizer with Sunscreen Broad Spectrum SPF 28 by

Drug Labeling and Warnings

Patricia Wexler Skin Brightening Daily Moisturizer with Sunscreen Broad Spectrum SPF 28 by is a Otc medication manufactured, distributed, or labeled by Bath & Body Works, Inc., Process Technologies & Packaging, LLC, Accel inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Avobenzone 1.8%, Octinoxate 7.5%, Octisalate 5.0%, Oxybenzone 2.4%

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 immediately.

DIRECTIONS

• apply liberally 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 the product in this container from excessive heat and direct sun.

INACTIVE INGREDIENTS

Water (Aqua, Eau), Butylene Glycol, Isostearyl Neopentanoate, Cetearyl Alcohol, Myristyl Nicotinate, Glycerin, Cyclopentasiloxane, Hydrogenated Lecithin, Arctostaphylos Uva Ursi Leaf Extract, Betula Alba Bark Extract, Morus Alba Leaf Extract, Pyrus Malus (Apple) Fruit Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Cinnamomum Cassia Bark Extract, Glycine Soja (Soybean) Seed Extract, Rheum Palmatum Root/Stalk Extract, Arbutin, Ascorbyl Glucoside, Tetrahexyldecyl Ascorbate, Urea, Sucrose, Xanthan Gum, Trehalose, Phospholipids, Sodium Hyaluronate, Palmitoyl Oligopeptide, Palmitoyl Tetrapeptide-7, Chrysin, Isononyl Isononanoate, Pentaerythrityl Tetraethylhexanoate, Cetearyl Glucoside, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Polysilicone-11, Dipotassium Glycyrrhizate, Steareth-20, Cyclohexasiloxane, Polyquaternium-51, Dimethylcyclohexylethoxy Isobutylpropanoate, Ethyl 2,2-Dimethylhydrocinnamal, Delphone, N-Hydroxysuccinimide, Sodium PCA, Carbomer, Triethanolamine, Methyldihydrojasmonate, Disodium EDTA, Cyclamen Aldehyde, Triacetin, Phenoxyethanol, Chlorphenesin, Methylparaben, Propylparaben, Butylparaben, Ethylparaben, Benzoic Acid, Isobutylparaben, Mica, Titanium Dioxide (CI 77891), Orange 4 (CI 15510), Yellow 5 (CI 19140), Red 4 (CI 14700).

COMPANY INFORMATION

Bath & Body Works, Distr.

Reynoldsburg, Ohio 43068

1-800-395-1001

www.bathandbodyworks.com

PRODUCT PACKAGING

INGREDIENTS AND APPEARANCE

PATRICIA WEXLER SKIN BRIGHTENING DAILY MOISTURIZER WITH SUNSCREEN BROAD SPECTRUM SPF 28 
avobenzone, octinoxate, octisalate, oxybenzone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62670-8042
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	1.8 g  in 100 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	7.5 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5.0 g  in 100 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	2.4 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62670-8042-6	50 mL in 1 JAR; Type 0: Not a Combination Product
2	NDC: 62670-8042-9	15 mL 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	08/28/2013

Labeler - Bath & Body Works, Inc. (878952845)

Establishment
Name	Address	ID/FEI	Business Operations
Process Technologies & Packaging, LLC		809172885	manufacture(62670-8042)

Establishment
Name	Address	ID/FEI	Business Operations
Accel inc.		838933430	relabel(62670-8042)