BioRelief Ice Pain Relieving description, usages, side effects, indications, overdosage, supplying and lots more!

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BioRelief Ice Pain Relieving

Mekt, LLC

BioRelief Ice Pain Relieving Spray




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredient                         Purpose

Menthol 10.00%.........................Topical analgesic

Purpose

Uses temporarily relieves minor pain associated with: -simple backache -muscle strains -sprains -bruises

Warnings For external use only

Uses

When using this product -use only as directed -avoid contact with eyes and mucous membrances -do not bandage tightly or use with a heating pad -do not apply to wounds or broken or irritated skin

Stop use and ask a doctor if -condition worsens -irritation develops -symptoms persist for more than 7 days, or if condition clears up and occurs again within a few days  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 right away.

Directions -adults and children over 18 years: spray directly onto affected area, repeat as necessary but no more than 4 times daily -children under 18 years: ask a doctor -wash hands with soap and water after applying

Inactive ingredients SD-Alcohol 40B, Aqua (Deionized Water), Isopropyl Alcohol, Dimethyl Sulfone (MSM), Glucosamine Sulfate, Chondroitin Sulfate, Mentha Piperita (Peppermint) Oil, Eucalyptus Globulus Oil, liex Paraguariensis Leaf Extract, Citric Acid, Arnica Montana Flower Extract, FD and C Blue #1

Distributed by MEKT, LLC, Boca Raton, FL 33432 www.BioFormulas.com  7 05105 34916 9

Bio Relief   ICE  PAIN RELIEVING SPRAY  With  ILEX  Arnica, MSM, Chondroitin, Glucosamine  Long Lasting, Deep Penetrating Pain Relief  -Arthritis -Muscles and Joints -Backache  Net Wt. 2 oz

BioRelief Ice Pain Relieving

BioRelief Ice Pain Relieving

MENTHOL SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:76019-100
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL 59 mL

Inactive Ingredients

Ingredient Name Strength
ALCOHOL
water
ISOPROPYL ALCOHOL
DIMETHYL SULFONE
GLUCOSAMINE SULFATE
PEPPERMINT OIL
CORYMBIA CITRIODORA LEAF OIL
CITRIC ACID MONOHYDRATE
ARNICA MONTANA FLOWER
FD&C BLUE NO. 1

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 59 in 1 BOTTLE
2 NDC:76019-100-02 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2011-02-14


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Be sure to consult your doctor before taking any medication!
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