LEAHUE MADHUCA TONIC- salicylic acid liquid

LEAHUE MADHUCA TONIC by

Drug Labeling and Warnings

LEAHUE MADHUCA TONIC by is a Otc medication manufactured, distributed, or labeled by Bio-interchange Co.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Salicylic Acid

Inactive Ingredients

Menthol, Water, Alcohol, etc

Purpose

Leahue Tonic helps to relieve the symptoms of hair loss, dandruff, and utching while provides a moist and shiny hair.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

Indications & Usage

Shake the product well before use. Spray an appropriate amount of product on your scalp and gently massage with your fingers to allow the product to be absorbed. Use two to three times per day.

Warnings (Cautions)

1. Stop use and ask a doctor incase. *condition worsens. *redness is present. *irritation develops.
2. Don’t apply to wounded or damaged skin.
3. When using this product. *use only as directed. *avoid contact with eyes.
4. Handle & Precautions 1) Keep out of reach of children. 2) For external use only. Store at room temperature.
5. If you have a history of allergic symptoms, consult your doctor and/or pharmacist before use.
6. Do not use this product on children under the age of three.
7. Persons who have hypersensitivity to salicylate, diabetes, poor blood circulation, kidney failure, infection, inflammation, skin abnormalities, and/or pregnant or likely to become pregnant should not use this product.

DOSAGE & ADMINISTRATION

For external use only

Label

INGREDIENTS AND APPEARANCE

LEAHUE MADHUCA TONIC 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72837-0003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.6 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
MENTHOL (UNII: L7T10EIP3A)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72837-0003-1	150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	04/01/2025

Labeler - Bio-interchange Co. (694235363)

Registrant - Bio-interchange Co. (694235363)

Establishment
Name	Address	ID/FEI	Business Operations
Bio-interchange Co.		694235363	manufacture(72837-0003)