POINT RELIEF COLD SPOT PAIN RELIEVING- menthol gel

国家: 美国

语言: 英文

来源: NLM (National Library of Medicine)

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产品特点 产品特点 (SPC)
25-01-2024

有效成分:

MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)

可用日期:

Fabrication Enterprises

给药途径:

TOPICAL

处方类型:

OTC DRUG

疗效迹象:

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

授权状态:

OTC monograph not final

产品特点

                                POINT RELIEF COLD SPOT PAIN RELIEVING- MENTHOL GEL
FABRICATION ENTERPRISES
----------
POINT RELIEF COLD SPOT PAIN RELIEVING GEL
_DRUG FACTS_
_ACTIVE INGREDIENTS:_
menthol - USP 12%
_PURPOSE:_
external analgesic
_USES:_
For temporary relief of minor aches and pains of the muscles and
joints associated with
simple backache, arthritis, bruises, strains, and/ or sprains.
_WARNINGS:_
For external use only
Avoid contact with eyes
DO NOT APPLY
to open wounds or damaged skin
If symptoms persist for more than sevan days, discontinue use and
consult
physician
KEEP OUT OF REACH OF CHILDREN
If swallowed, consult physician
Do not bandage tightly
_DIRECTIONS:_
Apply directly to affected area. Do not use more than four fimes per
day.
_OTHER INGREDIENTS:_
aqua (deionized water), arnica montana flower (arnica) extract,
boswellia serrata
extract, bromelain, carbomer, diazolidinyl urea, eucalyptus globulus
oil, glycyrrhiza
glabra (licorice) extract, ilex paraguariensis leaf (yerba mate)
extract, mentha piperita
(peppermint) oil, methyl salicylate, MSM (dimethyl sulfone),
polysorbate-80, propyl
paraben, propylene glycol, SD-alcohol 40B, triethanolamine
POINT RELIEF COLD SPOT PAIN RELIEVING GEL, 120ML (51452-035-01)
POINT RELIEF COLD SPOT PAIN RELIEVING GEL, 475ML (51452-035-02)
POINT RELIEF COLD SPOT PAIN RELIEVING GEL, 3.8L (51452-035-03)
POINT RELIEF COLD SPOT PAIN RELIEVING GEL, 420ML(HANDS
FREE)(51452-035-04)
POINT RELIEF COLD SPOT PAIN RELIEVING GEL, 950ML (51452-035-05)
POINT RELIEF COLD SPOT PAIN RELIEVING
menthol gel
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:51452-035
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)
MENTHOL
120 mg in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
Fabrication Enterprises
WATER (UNII: 059QF0KO0R)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
BROMELAINS (UNII: U182GP2CF3)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
DIAZOL
                                
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