COLD AND HOT MEDICATED PAIN RELIEF LARGE- menthol patch

Cold and Hot Medicated Pain Relief Large by

Drug Labeling and Warnings

Cold and Hot Medicated Pain Relief Large by is a Otc medication manufactured, distributed, or labeled by Valu Merchandisers Company, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Menthol 5%

Purpose

Topical analgesic

Uses

Temporarily relieves minor pain associated with:

• arthritis
• muscle strains
• simple backache
• bursitis
• cramps
• tendonitis
• muscle sprains
• bruises

Warnings

For external use only

When using this product

• 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

• 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,

ask a health professional before use.

Keep out of reach of children.

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

Directions

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

dihydroxyaluminum aminoacetate, glycerin, kaolin, methylparaben, polyacrylic acid, polyethylene glycol 400, polysorbate 80, povidone, propylparaben, purified water, sodium polyacrylate, tartaric acid, titanium dioxide

Questions or Comments?

call 1-800-883-0085

Reseal pouch after opening

package label

Best Choice Cold and Hot Large Medicated Patch

INGREDIENTS AND APPEARANCE

COLD AND HOT MEDICATED PAIN RELIEF LARGE 
menthol patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63941-949
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	875 mg

Inactive Ingredients
Ingredient Name	Strength
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
POVIDONE (UNII: FZ989GH94E)
DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)
GLYCERIN (UNII: PDC6A3C0OX)
KAOLIN (UNII: 24H4NWX5CO)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
WATER (UNII: 059QF0KO0R)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
POLYACRYLIC ACID (8000 MW) (UNII: 73861X4K5F)
TARTARIC ACID (UNII: W4888I119H)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63941-949-05	1 in 1 CARTON	12/29/2018
1		5 in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	09/12/2011

Labeler - Valu Merchandisers Company, Inc. (868703513)