AB 3000- benzalkonium chloride liquid

AB 3000 by

Drug Labeling and Warnings

AB 3000 by is a Otc medication manufactured, distributed, or labeled by Chemco, Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Benzalkonium Chloride...........0.13%

Inactive Ingredients 

Aloe Barbadensis Leaf Juice, Benzisothiazolinone, Caprylyl Glucoside, Citric Acid, Cocamide MIPA, Cocamidopropyl Betaine, Fragrance, Glycerine, Lauryl Glucoside, Maltodextrin, Methylisothiozolinone, PEG 150 Distearate, Red #40, Tetrasodium EDTA, Water, Yellow #5

Purpose

Antibacterial

Uses

For hand washing to decrease bacteria on the skin.

Warnings

For external use only.

When Using this Product

Avoid contact with eyes. If contat occurs, rinse eyes thoroughly with water.

Do not ingest. Stop use and contact a doctor if irritation and 

redness develop and conditions persist.

Keep out of reach of children.

If swallowed, get medical help

or contact Poison Control Center immediately.  

Directions

- Apply to wet hands. Work into lather and rinse thoroughly.

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

AB 3000 Hand Soap

INGREDIENTS AND APPEARANCE

AB 3000 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63039-1006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 kg  in 100 kg

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCERIN (UNII: PDC6A3C0OX)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
MAGNESIUM NITRATE (UNII: 77CBG3UN78)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
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: 63039-1006-2	1 in 1 BOX	12/29/2020
1	NDC: 63039-1006-1	3.80564 kg 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
unapproved drug other		12/29/2020

Labeler - Chemco (063798714)

Registrant - Chemco (063798714)

Establishment
Name	Address	ID/FEI	Business Operations
Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.		028311595	manufacture(63039-1006) , api manufacture(63039-1006) , pack(63039-1006)