CC USA NON-ALCOHOL FOAMING HAND SANITIZER- non-alcohol foaming hand sanitizer liquid

CC USA Non-Alcohol Foaming Hand Sanitizer by

Drug Labeling and Warnings

CC USA Non-Alcohol Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Coil Chem LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Acctive Ingredients

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Use(s)

For hand washing to help reduce bacteria that cause disease. For use when soap and water are not available.

Inactive Ingredients:

glycerin, decyl glucoside, purified water, aloe vera solution, citric acid.

Directions

Place enough product on hands to cover all surfaces. Rub hands together until dry. No rinsing required.

Supervise children under 6 years of age when using this product.

Warnings

For external use only

When using this product

Do not get into eyes. If contact offurs, rinse thoroughly with water.

Stop use and ask a doctor

if irritation and redness develop.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Package Label - Principal Display Panel

NDC: 75508-005-01 999349 mL

Package Label - Principal Display Panel

NDC: 75508-005-02 208198 mL

Package Label - Principal Display Panel

NDC: 75508-005-03 3785.41 mL

Package Label - Principla Display Panel

NDC: 75508-005-04 1892.7 mL

Package Label - Principal Display Panel

NDC: 75508-005-05 946.35 mL

Package Label - Principal Display Panel

NDC: 75508-005-06 473.18 mL

Package Label - Principal Display Panel

NDC: 75508-005-07 236.59 mL

Package Label - Principal Display Panel

NDC: 75508-005-08 177.4 mL

Package Label - Principal Display Panel

NDC: 75508-005-09 118.3 mL

Package Label - Principal Display Panel

NDC: 75508-005-10 59.1 mL

INGREDIENTS AND APPEARANCE

CC USA NON-ALCOHOL FOAMING HAND SANITIZER 
non-alcohol foaming hand sanitizer liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75508-005
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 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	2 mL  in 100 mL
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)	0.005 mL  in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.01 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	97.355 mL  in 100 mL
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)	0.5 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75508-005-01	999349 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product	09/01/2020
2	NDC: 75508-005-02	208198 mL in 1 DRUM; Type 0: Not a Combination Product	09/01/2020
3	NDC: 75508-005-03	3785.41 mL in 1 JUG; Type 0: Not a Combination Product	09/01/2020
4	NDC: 75508-005-04	1892.7 mL in 1 JUG; Type 0: Not a Combination Product	09/01/2020
5	NDC: 75508-005-05	946.35 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2020
6	NDC: 75508-005-06	473.18 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2020
7	NDC: 75508-005-07	236.59 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2020
8	NDC: 75508-005-08	177.4 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2020
9	NDC: 75508-005-09	118.3 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2020
10	NDC: 75508-005-10	59.1 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	09/01/2020

Labeler - Coil Chem LLC (963846535)

Establishment
Name	Address	ID/FEI	Business Operations
Coil Chem LLC		963846535	manufacture(75508-005)