UNIVERSAL ICE COLD ANALGESIC- menthol gel

Nchi: Marekani

Lugha: Kiingereza

Chanzo: NLM (National Library of Medicine)

Viambatanisho vya kazi:

Menthol 1.25%

Inapatikana kutoka:

Universal Distribution Center LLC

Njia ya uendeshaji:

TOPICAL

Dawa ya aina:

OTC DRUG

Matibabu dalili:

Topical Analgesic Temporary relieves of minor aches and pains in muscles and joints associated with - arthritis - simple backache - strains - bruises - sports injuries - sprains - condition worsens - symptoms last more than 7 days or clean up and occur again within a few days - redness or irritation develops

Idhini hali ya:

OTC monograph final

Tabia za bidhaa

UNIVERSAL ICE COLD ANALGESIC- MENTHOL GEL
UNIVERSAL DISTRIBUTION CENTER LLC
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UNIVERSAL ICE COLD ANALGESIC GEL
ACTIVE INGREDIENTS
Menthol 1.25%
PURPOSE
Topical Analgesic
USES
Temporary relieves of minor aches and pains in muscles and joints
associated with
arthritis
simple backache
strains
bruises
sports injuries
sprains
WARNINGS
FOR EXTERNAL USE ONLY
DO NOT USE
with other topical pain relievers
with heating pads or heating devices
WHEN USING THIS PRODUCT
do not use in or near the eyes
do not apply to wounds or damaged skin
do not bandage tightly
STOP USE AND ASK DOCTOR IF
condition worsens
symptoms last more than 7 days or clean up and occur again within a
few days
redness or irritation develops
IF PREGNANT OR BREAST-FEEDING,
ask a health professional before use
KEEP OUT OF THE REACH OF CHILDREN
If swallowed, get medical help or contact a Poison Control Center
immediately.
DIRECTIONS
clean affected area before applying products
adults and children 2 years of age and older
apply to affected area not more than 3 to 4 times daily.
INACTIVE INGREDIENTS
Water, Propylene glycol, Isopropyl alcohol, Carbomer, Sodium
hydroxide, Benzyl alcohol,
Edetate Disodium, Butylated hydroxytoluene, Camphor, Fd&c Blue No. 1
PRINCIPAL DISPLAY PANEL
ICE COLD
ANALGESIC GEL
8 FL.OZ (237 ml)
UNIVERSAL ICE COLD ANALGESIC
menthol gel
PRODUCT INFORMATION
Universal Distribution Center LLC
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:52000-106
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL -
UNII:L7T10EIP3A)
MENTHOL, UNSPECIFIED
FORM
1.25 g
in 100 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
BENZYL ALCOHOL (UNII: LKG8494WBH)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII:
4Q93RCW27E)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PROPYLENE GLYCOL (U