HUMCO TURPENTINE OIL RECTIFIED- turpentine liquid

Humco Turpentine Oil Rectified by

Drug Labeling and Warnings

Humco Turpentine Oil Rectified by is a Otc medication manufactured, distributed, or labeled by Humco Holding Group, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Turpentine Oil

Purpose

External Analgesic

Use

Warnings

For external use only.

Harmful or fatal if swallowed. Do not drink.

If swallowed stomach pumping and lavage may be required. Give edible oil or white mineral oil to drink.

Do not induce vomiting.

Avoid contact with eyes or mucous membranes.

Do not apply to wounds or damaged skin.

When using this product.

do not bandage.

Dicontinue use and consult a doctor if

condition worsens, or excessive irritation develops.

symptoms persist for more than 7 days, or clear up and occur again within a few days.

Keep out of the reach of children.

in case of accidental ingestion, seek professional assistance or contact a Poison Control Center right away. in case of eye contact, flush eyes with running water for 15 minutes, get medical attention.

Directions

Dilute 3 parts olive oil and mix well.

adults and children 2 yrs. and older: apply prparation to the affeced area not more than 4 times daily. Children under 2 yrs. of age: consult a doctor before use.

Other information

Flammable: Keep away from sparks, heat or flame.

Inactive ingredient

None

Principal display panel

label

INGREDIENTS AND APPEARANCE

HUMCO TURPENTINE OIL RECTIFIED 
turpentine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0395-2075
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TURPENTINE (UNII: XJ6RUH0O4G) (TURPENTINE - UNII:XJ6RUH0O4G)	TURPENTINE	1000 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0395-2075-92	59 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	03/12/2014	04/30/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	03/25/1998	04/30/2021

Labeler - Humco Holding Group, Inc. (825672884)

Establishment
Name	Address	ID/FEI	Business Operations
Humco Holding Group, Inc.		825672884	manufacture(0395-2075)