Take it above and Beyond Kit

Take it above and Beyond Kit by

Drug Labeling and Warnings

Take it above and Beyond Kit by is a Otc medication manufactured, distributed, or labeled by Global-C Nederland B.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

TAKE IT ABOVE AND BEYOND KIT- alcohol, benzalkonium chloride 
Global-C Nederland B.V.

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Take it above and Beyond Kit

Drug Facts

Active ingredient

Ethyl alcohol 65%

Purpose

Antiseptic

Use

For hand washing to decrease bacteria on the skin

Warnings

For external use only

Flammable, keep away from fire or flame.

Do not use

in the eyes

Stop use and ask a doctor if

  • irritation and redness develop
  • condition persists for more than 72 hours

Keep out of reach of children.

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

Directions

wet hands thoroughly with product and allow to dry without wiping

Other information

Store below 77 °F (25 °C)

Inactive ingredients

alpha tocopheryl acetate, monopropylene glycol, peg-7 glyceryl cocoate, polyacrylic acid, triclosan, triethanolamine, water

Drug Facts

Active ingredient

Benzalkonium Chloride 0.1%

Purpose

Antiseptic

Use

For hand washing to decrease bacteria on the skin

Warnings

For external use only

Flammable, keep away from fire or flame.

Do not use

in the eyes

Stop use and ask a doctor if

  • irritation and redness develop
  • condition persists for more than 72 hours

Keep out of reach of children.

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

Directions

wet hands thoroughly with product and allow to dry without wiping

Other information

Store below 77 °F (25 °C)

Inactive ingredients

Cellulose fiber, PEG-7 glyceryl cocoate, polyester fiber, water

Package Labeling:

Label

TAKE IT ABOVE AND BEYOND KIT 
alcohol, benzalkonium chloride kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 78657-007
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 78657-007-001 in 1 KIT09/12/202009/28/2023
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 BAG 3 mL
Part 21 PATCH 3 g
Part 1 of 2
ALCOHOL 
antiseptic hand sanitizer 65 ethyl gel
Product Information
Item Code (Source)NDC: 78657-002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.65 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
TRICLOSAN (UNII: 4NM5039Y5X)  
TROLAMINE (UNII: 9O3K93S3TK)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 78657-002-013 mL in 1 BAG; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)09/12/202009/28/2023
Part 2 of 2
ANTISEPTIC TOWEL BENZALKONIUM CHLORIDE 
benzalkonium chloride cloth
Product Information
Item Code (Source)NDC: 78657-006
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 78657-006-011 in 1 PACKAGE
13 g in 1 PATCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)09/12/202009/28/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)09/12/202009/28/2023
Labeler - Global-C Nederland B.V. (386762558)

Revised: 10/2023