GLOBAL CARE ICE COLD ANALGESIC- menthol ointment

GLOBAL CARE ICE COLD ANALGESIC by

Drug Labeling and Warnings

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

Drug Details [pdf]

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, arthrists, 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 a 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

GLOBAL CARE ICE COLD ANALGESIC 
menthol ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76176-089
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: 76176-089-01	227 g in 1 JAR; Type 0: Not a Combination Product	05/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	05/01/2018

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(76176-089)