Moisture Therapy

Manufacturer: Avon Products, Inc.
Effective date: 2014-10-02
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 22:40:26

Label at a glance#

ProductMoisture Therapy Anti-Itch

Active ingredientMenthol

Label structure7 sections

Contacts and useful links#

PhoneLabel contact1-800-FOR-AVON

PhoneLabel contact1-800-265-AVON

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient
Menthol 0.5 %......

OTC - PURPOSE SECTION

Purpose
.........External Analgesic

INDICATIONS & USAGE SECTION

Uses
For the temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, minor skin irritations.

WARNINGS SECTION

Warnings
For external use only

OTC - WHEN USING SECTION

When using this product

avoid contact with the eyes. If contact occurs, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if

condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days

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
Adults and children 2 years of age and older:

apply to affected area not more than 3 to 4 times daily

Children under 2 years of age:

consult a doctor before use

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
WATER/EAU, C12-15 ALKYL BENZOATE, ETHYLHEXYL PALMITATE, GLYCERIN, SD ALCOHOL 40-B, BUTYLENE GLYCOL, GLYCERYL STEARATE,
CETEARETH-20, AVENA SATIVA (OAT) MEAL EXTRACT, CITRIC ACID, CETEARETH-12, CETEARYL ALCOHOL, CETYL PALMITATE, CHOLESTEROL, CHLORPHENESIN, SODIUM HYDROXIDE, SODIUM DEHYDROACETATE.

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of PDPimage of DFBimage of DFBimage of DFB

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1314935	menthol 0.5 % Topical Spray	PSN	3
1314935	menthol 5 MG/ML Topical Spray	SCD	3
1314935	menthol 0.5 % Topical Spray	SY	3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
10096-0146-1	2020-01-31	C162847	48780-1	9d75b9d0-39ac-f424-e053-dadaa90a57ce	4ec3521a-893b-4082-8da3-062ba9cc0a1d

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
10096-0146-1	Moisture TherapyAnti-Itch	60 mL in 1 BOTTLE, SPRAY	SPRAY	60		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10096-0146	MOISTURE THERAPY ANTI-ITCH (MENTHOL) SPRAY [AVON PRODUCTS, INC.]	3	Legacy NDC, 1 package rows	20141003_4ec3521a-893b-4082-8da3-062ba9cc0a1d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
Menthol	ACTIVE INGREDIENT	L7T10EIP3A	3
Menthol	ACTIVE MOIETY	L7T10EIP3A	3

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

Moisture Therapy Anti-Itch
menthol

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
10096-0146	10096-0146-1

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
Menthol	L7T10EIP3A	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
2d0a0183-73a9-40a9-87e5-719b6989b434			4ec3521a-893b-4082-8da3-062ba9cc0a1d	2014-10-02	Warnings	Exact identifier spl id: 2d0a0183-73a9-40a9-87e5-719b6989b434 spl set id: 4ec3521a-893b-4082-8da3-062ba9cc0a1d

Reported adverse events (FAERS/openFDA)#

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