EAGLE MEDICATED- menthol methyl salicylate oil

Eagle by

Drug Labeling and Warnings

Eagle by is a Otc medication manufactured, distributed, or labeled by Borden Company (Private) Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Menthol 14.5%
Methyl Salicylate 30%

Purpose

Topical Analgesic

Topical Analgesic

Uses

temporarily relieves the minor aches and pains of muscle and joint associated with : ■simple backache ■ strains ■ bruises ■ sprains

Warning

For external use only

Do not use

■ on woulds or damaged skin ■ with a heating pad

When using this product

■ avoid contact with eyes or mucous membranes

■ do not bandage tightly

Stop use and ask a doctor if

■ condition worsens or symptoms persist for more than 7 days ■ symptoms clear up and occur again within a few days ■ excessive skin irritation occurs

Keep this drug out of reach of children

To avoid accidental poisoning, if swallowed, get medical help or contact a Poison Control Center right away.

Directions

■ Use only as directed ■ adults and children 2 years and older: apply to affected area not more than 3 to 4 time daily. ■ children under 2 years of age: ask a doctor

Inactive ingredients

D&C Green No. 6, D&C Yellow No. 11, ethyl alcohol, mineral oil, rose oil

Question?

1-800-777-6717 or 1-800-645-0789

Package Label

INGREDIENTS AND APPEARANCE

EAGLE  MEDICATED
menthol methyl salicylate oil

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43405-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	14.5 g  in 100 mL
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	30 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
D&C YELLOW NO. 11 (UNII: 44F3HYL954)
ALCOHOL (UNII: 3K9958V90M)
MINERAL OIL (UNII: T5L8T28FGP)
ROSE OIL (UNII: WUB68Y35M7)
D&C GREEN NO. 6 (UNII: 4QP5U84YF7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43405-005-08	1 in 1 BOX	03/04/2022
1		8 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	03/04/2022

Labeler - Borden Company (Private) Limited (595109711)

Establishment
Name	Address	ID/FEI	Business Operations
Borden Company (Private) Limited		595109711	manufacture(43405-005)