PHARMACYS PRESCRIPTION ICE COLD ANALGESIC- menthol ointment

PHARMACYS PRESCRIPTION ICE COLD ANALGESIC by

Drug Labeling and Warnings

PHARMACYS PRESCRIPTION ICE COLD ANALGESIC by is a Otc medication manufactured, distributed, or labeled by Ningbo Liyuan Daily Chemical Products Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts Active Ingredient

Menthol 1 percent

Purpose

Pain relieving gel

Uses:

For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises, sprains

Warnings

For external use only.

When using this product

• avoid contact with the eyes
• do not handage tightly
• do not apply to wounds or damaged skin
• do not use with heating pads or other heating devices

Stop use and ask doctor if

condition worsens, or if symptoms persist for more than 7 days or clear up and occur again with a few days. (see other side panel)

Keep out of reach of children.

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

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: do not use, consult a doctor

Other Information

Do Not Freeze

Inactive Ingredients

carbomer, isopropyl alcohol, nonyl phenyl polyoxyethylene ether, camphor, kathon CG, FD&C blue no.1, triethanolamine, water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PHARMACYS PRESCRIPTION ICE COLD ANALGESIC 
menthol ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76176-113
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
TRIETHANOLAMINE BENZOATE (UNII: M3EN4GC19W)
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
CARBOMER 934 (UNII: Z135WT9208)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76176-113-01	227 g in 1 JAR; Type 0: Not a Combination Product	08/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	08/01/2018

Labeler - Ningbo Liyuan Daily Chemical Products Co., Ltd. (530766098)

Registrant - Ningbo Liyuan Daily Chemical Products Co., Ltd. (530766098)

Establishment
Name	Address	ID/FEI	Business Operations
Ningbo Liyuan Daily Chemical Products Co., Ltd.		530766098	manufacture(76176-113)