BIGELOIL® LIQUID GEL

BIGELOIL® LIQUID GEL

Drug Labeling and Warnings

Drug Details

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BIGELOIL- menthol gel 
W. F. Young, Inc.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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BIGELOIL®
LIQUID GEL

Can be used before, during and after competition

Can also be used on dogs

Indications

For temporary relief of minor pain and swelling from sprains, strains, bruises, arthritis, overworked muscles and minor wounds.

Directions for Use

Rub onto sore area 3 to 4 times a day. For faster relief, rub with hair and wrap or blanket. For minor cuts and scrapes apply without rubbing.

Caution: Avoid contact with eyes and mucous membranes.

Stop using if skin irritation develops or symptoms persist for more than 10 days.

For severe injuries consult a veterinarian.

For external use only. Keep out of reach of children.

Warning

Flammable. Keep away from fire, sparks and heated surfaces.

Store at room temperature.

For animal use only.

Active Ingredient

Menthol 2%. Also contains Alcohol: 60%.

Distributed by:
W. F. Young, Inc.
302 Benton Drive
E. Longmeadow, MA 01028 USA
© WFY
www.absorbine.com
RM 342360-5

PRINCIPAL DISPLAY PANEL - 414 mL Bottle Label

BIGELOIL®
LIQUID GEL

Reduces Pain & Swelling of Sore
Muscles, Joints, Legs & Arthritis

Excellent Under Wraps

TOPICAL PAIN RELIEF GEL

HERBAL FORMULA

14 fl oz. (414 mL)

PRINCIPAL DISPLAY PANEL - 414 mL Bottle Label
BIGELOIL 
menthol gel
Product Information
Product TypeOTC ANIMAL DRUGItem Code (Source)NDC: 11444-136
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Menthol, Unspecified Form (UNII: L7T10EIP3A) (Menthol, Unspecified Form - UNII:L7T10EIP3A) Menthol, Unspecified Form2 g  in 112 mL
Inactive Ingredients
Ingredient NameStrength
Alcohol (UNII: 3K9958V90M)  
Thymol (UNII: 3J50XA376E)  
Methyl Salicylate (UNII: LAV5U5022Y)  
Water (UNII: 059QF0KO0R)  
Glycerin (UNII: PDC6A3C0OX)  
Polysorbate 80 (UNII: 6OZP39ZG8H)  
FD&C yellow No. 5 (UNII: I753WB2F1M)  
D&C Green No. 5 (UNII: 8J6RDU8L9X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 11444-136-01414 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved drug other01/01/1997
Labeler - W. F. Young, Inc. (001114669)

Revised: 3/2016
 
W. F. Young, Inc.


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