PONDS LUMINOUS MOISTURE DAY SPF 15- avobenzone, ensulizole, octicsalate lotion

Ponds by

Drug Labeling and Warnings

Ponds by is a Otc medication manufactured, distributed, or labeled by CONOPCO Inc. d/b/a Unilever, Marietta Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients
AVOBENZONE (3.0%)
ENSULIZOLE (1.0%)
OCTISALATE (5.0%)

PURPOSE

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 to face and neck 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 10a.m. - 2p.m.
· wear long-sleeved shirts, pants, hats, and sunglasses

INACTIVE INGREDIENT

Inactive ingredients
Water/Agua
Glycerin
Stearic Acid
Glycol Stearate
PEG-100 Stearate
Dimethicone
Glyceryl Stearate
Carbomer
Caprylyl Glycol
Cetyl Alcohol
Xanthan Gum
Fragrance/Fragancia
Stearamide AMP
Potassium Stearate
Phenoxyethanol
Disodium EDTA
Methylisothiazolinone
Mica

QUESTIONS

Questions or comments?
Call toll free 1-800-909-9493

PRINCIPAL DISPLAY PANEL

PDP

PRINCIPAL DISPLAY PANEL

Carton

INGREDIENTS AND APPEARANCE

PONDS  LUMINOUS MOISTURE DAY SPF 15
avobenzone, ensulizole, octicsalate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64942-1288
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3.0 g  in 100 mL
ENSULIZOLE (UNII: 9YQ9DI1W42) (ENSULIZOLE - UNII:9YQ9DI1W42)	ENSULIZOLE	1.0 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5.0 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
STEARIC ACID (UNII: 4ELV7Z65AP)
GLYCOL STEARATE (UNII: 0324G66D0E)
PEG-100 STEARATE (UNII: YD01N1999R)
DIMETHICONE (UNII: 92RU3N3Y1O)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
POTASSIUM STEARATE (UNII: 17V812XK50)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CETYL ALCOHOL (UNII: 936JST6JCN)
XANTHAN GUM (UNII: TTV12P4NEE)
STEARAMIDE AMP (UNII: U3K8640346)
MICA (UNII: V8A1AW0880)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64942-1288-2	1 in 1 CARTON
1	NDC: 64942-1288-1	59 mL in 1 TUBE
2	NDC: 64942-1288-4	1 in 1 CARTON
2	NDC: 64942-1288-3	50 mL in 1 TUBE
3	NDC: 64942-1288-6	1 in 1 PACKAGE
3	NDC: 64942-1288-5	4.4 mL in 1 PACKET

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	08/01/2012

Labeler - CONOPCO Inc. d/b/a Unilever (001375088)

Establishment
Name	Address	ID/FEI	Business Operations
Marietta Corporation		111359712	pack(64942-1288)