Best Choice Cold & Hot Large Medicated Patch

Manufacturer: Valu Merchandisers Company, Inc.
Effective date: 2022-07-06
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:50:06

Label at a glance#

ProductCold and Hot Medicated Pain Relief Large

Active ingredientMENTHOL

Label structure8 sections

Indications and uses

Temporarily relieves minor pain associated with: arthritis muscle strains simple backache bursitis cramps tendonitis muscle sprains bruises

Dosage and administration

Adults and children over 12 years: carefully remove backing from patch apply one patch to affected area repeat as necessary, but no more than 4 times daily Children under 12 years of age : Ask a doctor

Contacts and useful links#

PhoneLabel contact1-800-883-0085

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 5%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves minor pain associated with:

arthritis
muscle strains
simple backache
bursitis
cramps
tendonitis
muscle sprains
bruises

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

use only as directed
do not bandage tightly or use with heating pad
avoid contact with eyes and mucous membranes
do not apply to wounds or damaged skin
do not use if you are allergic to any ingredients of this product

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worsens
symptoms persist for more than 7 days or clear up and occur again within a few days
redness is present
irritation develops

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children over 12 years:

carefully remove backing from patch
apply one patch to affected area
repeat as necessary, but no more than 4 times daily

Children under 12 years of age: Ask a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

carboxymethylcellulose, dihydroxyaluminum aminoacetate, glycerin, kaolin, methylparaben, mineral oil, petrolatum, polyacrylic acid, polysorbate 80, propylene glycol, povidone, propylparaben, sodium polyacrylate, tartaric acid, titanium dioxide, water

Questions or Comments?

OTC - QUESTIONS SECTION

call 1-800-883-0085

Reseal pouch after opening

package label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Best Choice Cold and Hot Large Medicated Patch

image of carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
420222	menthol 5 % Medicated Patch	PSN	1
420222	menthol 0.05 MG/MG Medicated Patch	SCD	1
420222	menthol 5 % Medicated Patch	SY	1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
f52be47f-7aa7-46c0-b1fa-50c18dd50206	Product name	1	20201029

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63941-948-05	2024-01-30	C162847	48780-1	1030e365-6491-111a-e063-dadaa90a10e2	Best Choice Cold & Hot Large Medicated Patch

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63941-948-05	Cold and Hot Medicated Pain Relief Large	5 in 1 POUCH	PATCH	5		1
63941-948-05	Cold and Hot Medicated Pain Relief Large	1 in 1 CARTON	PATCH	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63941-948	COLD AND HOT MEDICATED PAIN RELIEF LARGE (MENTHOL) PATCH [VALU MERCHANDISERS COMPANY, INC.]	1	Legacy NDC, 2 package rows	20220708_e32e0eca-81d7-7986-e053-2a95a90ae6e1.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

Cold and Hot Medicated Pain Relief Large
Menthol
PETROLATUM
SODIUM POLYACRYLATE (8000 MW)
POVIDONE
DIHYDROXYALUMINUM AMINOACETATE
GLYCERIN
KAOLIN
METHYLPARABEN
CARBOXYMETHYLCELLULOSE
POLYSORBATE 80
WATER
POLYETHYLENE GLYCOL 400
POLYACRYLIC ACID (8000 MW)
TARTARIC ACID
TITANIUM DIOXIDE
PROPYLPARABEN
MINERAL OIL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
63941-948	63941-948-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PETROLATUM	4T6H12BN9U	IACT
SODIUM POLYACRYLATE (8000 MW)	285CYO341L	IACT
POVIDONE	FZ989GH94E	IACT
DIHYDROXYALUMINUM AMINOACETATE	DO250MG0W6	IACT
GLYCERIN	PDC6A3C0OX	IACT
KAOLIN	24H4NWX5CO	IACT
METHYLPARABEN	A2I8C7HI9T	IACT
CARBOXYMETHYLCELLULOSE	05JZI7B19X	IACT
POLYSORBATE 80	6OZP39ZG8H	IACT
WATER	059QF0KO0R	IACT
POLYETHYLENE GLYCOL 400	B697894SGQ	IACT
POLYACRYLIC ACID (8000 MW)	73861X4K5F	IACT
TARTARIC ACID	W4888I119H	IACT
TITANIUM DIOXIDE	15FIX9V2JP	IACT
MENTHOL	L7T10EIP3A	ACTIB
PROPYLPARABEN	Z8IX2SC1OH	IACT
MINERAL OIL	T5L8T28FGP	IACT

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
e32e0edf-ec5e-b707-e053-2a95a90a4e82			e32e0eca-81d7-7986-e053-2a95a90ae6e1	2022-07-06	Warnings	Exact identifier spl id: e32e0edf-ec5e-b707-e053-2a95a90a4e82 spl set id: e32e0eca-81d7-7986-e053-2a95a90ae6e1

Reported adverse events (FAERS/openFDA)#

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