STOP HAIR- citric acid monohydrate spray

stop hair by

Drug Labeling and Warnings

stop hair by is a Otc medication manufactured, distributed, or labeled by MILA BEAUTY PTY LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Citric Acid Monohydrate  7mg/ml (0.7 % w/v)

Purpose

HAIR REDUCING SPRAY

Keep Out of Reach of Children.

Keep Out of Reach of Children.

Indication and Usage

STOPHAIR is a blend of natural ingredients, including plant extracts, and may assist in naturally minimising hair regrowth over time, potentially eliminating the need for the continual use of intrusive, expensive and time-consuming methods of hair removal.

Inactive Ingredients

aqua, chelidonium majus (celandine) extract, larrea divaricata (chaparel) extract, glycerol, olea eurapaea extract, almond extract.

Dosage & Administration

DIRECTIONS FOR USE

Apply STOPHAIR directly onto the skin twice a day (morning and night) for 5 consecutive days after hair removal, and continue once a day thereafter. Repeat this process every time after hair removal.

STOPHAIR can be used with any conventional method of hair removal, including waxing, laser, shaving, depilatory creams and electrolysis.

WARNINGS

Use only as directed. Perform a 48 hour patch test prior to use. If irritation occurs, discontinue use.

Product Label

INGREDIENTS AND APPEARANCE

STOP HAIR 
citric acid monohydrate spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50965-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL)	ANHYDROUS CITRIC ACID	7 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
ALMOND (UNII: 3Z252A2K9G)
CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
LARREA TRIDENTATA LEAF (UNII: PK0TXD049P)
OLEA EUROPAEA WHOLE (UNII: 769297N5OK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50965-001-10	125 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/01/2012

Labeler - Mila Beauty Pty Ltd (747409113)

Establishment
Name	Address	ID/FEI	Business Operations
Mila Beauty Pty Ltd		747409113	manufacture(50965-001) , pack(50965-001)