MAGICSHINE ANTIBACTERIAL FOAMING HAND- benzalkonium chloride liquid

MAGICSHINE ANTIBACTERIAL FOAMING HAND by

Drug Labeling and Warnings

MAGICSHINE ANTIBACTERIAL FOAMING HAND by is a Otc medication manufactured, distributed, or labeled by Maintex, Morgan Gallacher Inc DBA Custom Chemical Formulators Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Benzalkonium Chloride.......0.13%

Purpose

Antiseptic

Uses

For hand washing to decrease bacteria on the skin.

Warnings

For external use only.

When Using this Product

- Avoid contact with the eyes.

- If contact occurs, rinse eyes thoroughly with water. Do not ingest.

- Stop use and contact a doctor if irritation and redness develop

  and if conditions persist.

Keep out of reach of children.

Keep out of reach of children. If swallowed, get medical help

or contact a Poison Control Center immediately.

Directions

-Apply to wet hands, work into a lather and rinse thoroughly.

-Children under 6 years of age should be supervised when using this product.

Inactive Ingredients

ALOE VERA LEAF, CAPRYLYL/CAPRYL OLIGOGLUCOSIDE, ANHYDROUS CITRIC ACID, COCAMIDOPROPYL BETAINE, GLYCERIN, LAURYL GLUCOSIDE, MAGNESIUM NITRATE, MALTODEXTRIN, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, FD&C RED NO. 40, EDETATE SODIUM, WATER, FD&C YELLOW NO. 5

MagicShine Antibacterial Foaming Hand Soap

MagicShine Antibacterial Foaming Hand Soap

INGREDIENTS AND APPEARANCE

MAGICSHINE ANTIBACTERIAL FOAMING HAND 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77617-012
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	.13 g  in 0.1 L

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCERIN (UNII: PDC6A3C0OX)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
MAGNESIUM NITRATE (UNII: 77CBG3UN78)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C RED NO. 40 (UNII: WZB9127XOA)
EDETATE SODIUM (UNII: MP1J8420LU)
WATER (UNII: 059QF0KO0R)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77617-012-02	1 in 1 BOX	09/18/2018
1	NDC: 77617-012-01	3.785 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M	09/18/2018

Labeler - Maintex (008317307)

Registrant - Maintex (008317307)

Establishment
Name	Address	ID/FEI	Business Operations
Morgan Gallacher Inc DBA Custom Chemical Formulators Inc		028311595	manufacture(77617-012) , api manufacture(77617-012) , pack(77617-012)