Humco Turpentine Oil Rectified

Manufacturer
Humco Holding Group, Inc.
Effective date
2020-02-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:41:10

Label at a glance#

ProductHumco Turpentine Oil Rectified
Active ingredientTURPENTINE
Label structure11 sections

Dosage and administration

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.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Turpentine Oil

Purpose

OTC - PURPOSE SECTION

External Analgesic

Warnings

WARNINGS SECTION

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.

OTC - WHEN USING SECTION

do not bandage.

Dicontinue use and consult a doctor if

OTC - ASK DOCTOR SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

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

OTHER SAFETY INFORMATION

Flammable: Keep away from sparks, heat or flame.

Inactive ingredient

INACTIVE INGREDIENT SECTION

None

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

image descriptionimage description

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0395-2075-92ML - Milliliter0395-207518be81c5-2459-4ce3-98b0-5e6d8c87e3ff12014-04-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
TURPENTINEACTIVE INGREDIENTXJ6RUH0O4G1
TURPENTINEACTIVE MOIETYXJ6RUH0O4G1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0395-20750395-2075-92

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
TURPENTINEXJ6RUH0O4GACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
9e7d36fd-6177-422c-e053-2995a90a5a378ddbf86a-434f-4b42-8a40-085c684b56882020-02-13WarningsExact identifier
spl id: 9e7d36fd-6177-422c-e053-2995a90a5a37
spl set id: 8ddbf86a-434f-4b42-8a40-085c684b5688

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.