BIGELOIL- menthol liquid

Bigeloil by

Drug Labeling and Warnings

Bigeloil by is a Animal medication manufactured, distributed, or labeled by W. F. Young, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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 2 to 3 times a day. For faster relief, rub with hair and wrap or blanket, especially overnight. Body Wash: mix 2 to 4 oz. with 1 gal. water, apply with sponge, avoid eyes. Brace: mix 2 to 3 oz. with 1 quart water, apply with sponge to warm horse up before workout, avoid eyes and saddle area. Arthritis: rub onto knees, hocks and fetlocks before workout, apply again at night and lightly wrap. Antiseptic: for minor wounds and skin irritations, apply full strength 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 Ingredients

Menthol 1.25% W/W.

Other Ingredients

Alcohol, D&C Green #5, FD&C Yellow #5, Fragrance, Juniperberry Oil, Methyl Salicylate, Salicylic Acid, Thymol and Purified Water.

SPL UNCLASSIFIED SECTION

Distributed by:
W. F. Young, Inc.
302 Benton Drive
E. Longmeadow, MA 01028 USA
© WFY
www.absorbine.com
RM 342328-3

PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label

BIGELOIL®

THE PROFESSIONAL'S LINIMENT

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

Excellent Under Wraps

TOPICAL PAIN
RELIEF LIQUID

16 fl oz. (473 mL)

INGREDIENTS AND APPEARANCE

BIGELOIL 
menthol liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 11444-130
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	1.25 g  in 115 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11444-130-01	473 mL in 1 BOTTLE, PLASTIC
2	NDC: 11444-130-02	946 mL in 1 BOTTLE, PLASTIC
3	NDC: 11444-130-03	3785 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
UNAPPROVED DRUG OTHER		01/01/1997

Labeler - W. F. Young, Inc. (001114669)