VAMOUSSE LICE DEFENSE- eucalyptus globulus, natrum muriaticum shampoo

Vamousse Lice Defense by

Drug Labeling and Warnings

Vamousse Lice Defense by is a Homeopathic medication manufactured, distributed, or labeled by Alliance Pharma Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Eucalyptus globulus 2X (HPUS)

Natrum muriaticum 2X (HPUS)

Purpose

Pediculicide

Uses

For daily defense against head lice infestations.

Warnings

For external use only.

Do not use near eyes inside nose or mouth on eyebrows or eyelashes. See a doctor if lice are present in these areas. Do not use if you have ever had an allergic reaction to this product or any of its ingredients.

When using this product:

Do not use in or near the eyes. Close eyes while applying.

Do not permit contact with mucous membranes, such as inside the nose, as irritation or stinging may occur.

Stop use and ask a doctor if eye irritation occurs skin or scalp irritation or infection occurs.

If pregnant or breast-feeding,ask a health professional before use.

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Directions:

Adults and children 2 years and older:

Apply a generous amount of shampoo to wet hair, work into a lather and massage into scalp. Leave shampoo in hair for at least 3 minutes. Rinse.

For defense against a head lice infestation, use daily for at least 10 to 14 days to kill any lice that may have hatched.

For an active head lice infestation, use Vamousse ®Lice Treatment before using this shampoo.

Children under 2 years: ask a doctor.

Product may be used as often as needed.

Inactive Ingredients

Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Sodium Cocoyl Isethionate, Cocamide DIPA, Benzyl Alcohol, Butyl Lactate, Citric Acid Anhydrous, Polyquaternium-10, Tetrasodium EDTA, Propylene Glycol, Diazolidinyl Urea, Iodopropynyl Butylcarbamate, PEG-150 Pentaerythrityl Tetrastearate, PEG-6 Caprylic/Capric Glycerides, Tea Tree Oil, Eucalyptus Oil, Geraniol, Isopropyl myristate, Fragrance

Questions?

1.855.373.7210 or www.VamousseLice.com

Call to report serious side effects

SPL UNCLASSIFIED SECTION

NEW

PESTICIDE - FREE

Kill Stray Super Lice*

Before Detected

with Tea Tree Oil

Defends Family Against Lice Infestation

CLINICALLY PROVEN

Use After Exposure or Treatment

Follow-up with Favorite Conditioner

No Parabens, Sulfates or Dyes

HOMEOPATHIC

*As shown in lab studies

Manufactured for: ALLIANCE

Alliance Pharma Inc., Cary, NC 27518

Made in the U.S.A Vamousse, Alliance and associated devices are trade marks of Alliance Pharmaceuticals Limited

Packaging

INGREDIENTS AND APPEARANCE

VAMOUSSE LICE DEFENSE 
eucalyptus globulus, natrum muriaticum shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72238-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (EUCALYPTUS GLOBULUS LEAF - UNII:S546YLW6E6)	EUCALYPTUS GLOBULUS LEAF	2 [hp_X]  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	2 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
PEG-150 PENTAERYTHRITYL TETRASTEARATE (UNII: 8L4OOQ76AM)
CAPRYLOCAPROYL POLYOXYLGLYCERIDES 6 (UNII: GO50W2HWO8)
COCO DIISOPROPANOLAMIDE (UNII: S485AM948Q)
TEA TREE OIL (UNII: VIF565UC2G)
BENZYL ALCOHOL (UNII: LKG8494WBH)
EUCALYPTUS OIL (UNII: 2R04ONI662)
BUTYL LACTATE (UNII: 0UI63W814U)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
POLYQUATERNIUM-10 (125 MPA.S AT 2%) (UNII: L45WU8S981)
GERANIOL (UNII: L837108USY)
EDETATE SODIUM (UNII: MP1J8420LU)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72238-004-01	295 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2021
2	NDC: 72238-004-03	400 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2021
3	NDC: 72238-004-05	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2021
4	NDC: 72238-004-02	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/01/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		05/01/2021

Labeler - Alliance Pharma Inc. (081138954)