FDA.reportPublic FDA data

Moisture Therapy

Manufacturer
Avon Products, Inc
Effective date
2013-02-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:34:46

Label at a glance#

ProductMoisture Therapy Daily Skin Defense Body
Active ingredientOCTINOXATE, OCTISALATE, OXYBENZONE
Label structure8 sections

Storage and handling

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

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients
Octinoxate, 7.5%.............
Octisalate, 5.0%...............
Oxybenzone, 1.0% ..............

OTC - PURPOSE SECTION

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

INDICATIONS & USAGE SECTION

Uses

  • helps prevent sunburn

WARNINGS SECTION

Warnings
Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.
For external use only

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions

  • apply generously and evenly 15 minutes before sun exposure
  • children under 6 month of age:ask a doctor
  • reapply at least every 2 hours
  • use a water resistant sunscreen if swimming or sweating

STORAGE AND HANDLING SECTION

Other Information

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

INACTIVE INGREDIENT SECTION

Inactive ingredients:
WATER/EAU, GLYCERIN, BUTYLENE GLYCOL, GLYCERYL STEARATE, PEG-8, SILICA, CETYL ALCOHOL, IMIDAZOLIDINYL UREA, METHYLPARABEN, CARBOMER, DIMETHICONE, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, DISODIUM EDTA, HYDROGENATED LECITHIN, PARFUM/FRAGRANCE, SODIUM HYDROXIDE, POLYGLYCERYL-3 DIISOSTEARATE, ORYZA SATIVA (RICE) BRAN OIL, DIMETHICONOL, HYDROGENATED POLYISOBUTENE, ASCORBYL PALMITATE, PANTHENOL, SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, TOCOPHERYL ACETATE,
RETINYL PALMITATE, GLYCINE SOJA (SOYBEAN) STEROLS, LECITHIN, GLYCINE SOJA (SOYBEAN) OIL, TOCOPHEROL.

OTC - QUESTIONS SECTION

Questions or comments?
Call 1-800-FOR-AVON or 1-800-265-AVON in Canada.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of PDPimage of PDPimage of labelimage of labelimage of labelimage of label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10096-0291-12019-11-27C16284748780-19855d018-e9cf-cd31-e053-dbdaa90ab51a74fadef2-f5fd-49fd-9b54-dbaa36547ed4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10096-0291-1Moisture TherapyDaily Skin Defense Body400 mL in 1 BOTTLELOTION4002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10096-0291MOISTURE THERAPY DAILY SKIN DEFENSE BODY (OCTINOXATE, OCTISALATE, OXYBENZONE) LOTION [AVON PRODUCTS, INC]2Legacy NDC, 1 package rows20130301_74fadef2-f5fd-49fd-9b54-dbaa36547ed4.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD512
OCTISALATEACTIVE INGREDIENT4X49Y0596W2
OXYBENZONEACTIVE INGREDIENT95OOS7VE0Y2
OCTINOXATEACTIVE MOIETY4Y5P7MUD512
OCTISALATEACTIVE MOIETY4X49Y0596W2
OXYBENZONEACTIVE MOIETY95OOS7VE0Y2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10096-029110096-0291-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB
OXYBENZONE95OOS7VE0YACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
9baffd63-26a9-4a6e-8e1b-95b02edba76b74fadef2-f5fd-49fd-9b54-dbaa36547ed42013-02-27WarningsExact identifier
spl id: 9baffd63-26a9-4a6e-8e1b-95b02edba76b
spl set id: 74fadef2-f5fd-49fd-9b54-dbaa36547ed4

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.