FDA.reportPublic FDA data

Moisture Therapy

Manufacturer
Avon Products, Inc.
Effective date
2010-09-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:25:51

Label at a glance#

ProductMoisture Therapy Ultra Skin Renewal
Active ingredientPetrolatum
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient
Petrolatum 60.3%...........................

OTC - PURPOSE SECTION

                   Purpose
........................Skin protectant

INDICATIONS & USAGE SECTION

Uses
• temporarily protects minor: • cuts • scrapes • burns
• helps prevent, temporarily protects and helps relieve chafed,
chapped or cracked skin
• helps prevent and protect from the drying effects of wind and cold
weather

WARNINGS SECTION

Warnings
For external use only

OTC - WHEN USING SECTION

When using this product
• do not get into eyes

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if
• condition worsens
• symptoms last more than 7 days or clear up and occur again within
a few days

OTC - DO NOT USE SECTION

Do not use on
• deep or puncture wounds
• animal bites
• serious burns

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 as needed

INACTIVE INGREDIENT SECTION

Inactive ingredients ETHYLHEXYL PALMITATE, C14-22 ALKANE, CERESIN,
C12-13 ALKYL LACTATE, C18-38 ALKYL HYDROXYSTEAROYL STEARATE,
GLYCERYL CAPRYLATE, BUTYROSPERMUM PARKII (SHEA) BUTTER, HELIANTHUS
ANNUUS (SUNFLOWER) SEED OIL, SALICYLIC ACID, ORYZA SATIVA
(RICE) BRAN OIL, JOJOBA ESTERS, HYDROGENATED POLYISOBUTENE,
BISABOLOL, GLYCINE SOJA (SOYBEAN)
STEROLS, LECITHIN, GLYCINE
SOJA (SOYBEAN) OIL, TOCOPHEROL.

OTC - QUESTIONS SECTION

Questions? Call 1-800-FOR-AVON

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of PDPimage of PDPimage of labelimage of label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1098373petrolatum 60.3 % Topical OintmentPSN1
1098373petrolatum 0.603 MG/MG Topical OintmentSCD1
1098373petrolatum 60.3 % Topical OintmentSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10096-0228-12019-10-21C16284748780-1956f9ecf-cae6-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10096-0228-1Moisture TherapyUltra Skin Renewal100 mL in 1 TUBEOINTMENT1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10096-0228MOISTURE THERAPY ULTRA SKIN RENEWAL (PETROLATUM) OINTMENT [AVON PRODUCTS, INC.]1Legacy NDC, 1 package rows20100919_44ed4e04-2d65-4d6a-8314-783dba154850.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
PetrolatumACTIVE INGREDIENT4T6H12BN9U1
PETROLATUMACTIVE MOIETY4T6H12BN9U1
CERESININACTIVE INGREDIENTQ1LS2UJO3A1
ETHYLHEXYL PALMITATEINACTIVE INGREDIENT28659933091
GLYCERYL CAPRYLATEINACTIVE INGREDIENTTM2TZD4G4A1
SALICYLIC ACIDINACTIVE INGREDIENTO414PZ4LPZ1

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10096-022810096-0228-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
Petrolatum4T6H12BN9UACTIB
ETHYLHEXYL PALMITATE2865993309IACT
CERESINQ1LS2UJO3AIACT
GLYCERYL CAPRYLATETM2TZD4G4AIACT
SALICYLIC ACIDO414PZ4LPZIACT

Source Document#

Source XML · Source PDF

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 4 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
CERESINCERESINQ1LS2UJO3ACREAM / VAGINAL280 mgExact identifier — unii candidate
2 equally ranked IID candidates
GLYCERYL CAPRYLATEGLYCERYL MONOCAPRYLATETM2TZD4G4ATABLET / ORAL1 mgExact identifier — unii candidate
2 equally ranked IID candidates
GLYCERYL CAPRYLATEGLYCERYL MONOCAPRYLATETM2TZD4G4ACAPSULE / ORAL400 mgExact identifier — unii candidate
2 equally ranked IID candidates
CERESINCERESINQ1LS2UJO3AOINTMENT / TOPICAL1097 mgExact identifier — unii candidate
2 equally ranked IID candidates

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
f292780e-524a-4a00-b306-db9087e7ce8344ed4e04-2d65-4d6a-8314-783dba1548502010-09-17WarningsExact identifier
spl id: f292780e-524a-4a00-b306-db9087e7ce83
spl set id: 44ed4e04-2d65-4d6a-8314-783dba154850

Reported adverse events (FAERS/openFDA)#

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