HOLLADAY HELPING HANDS- antiseptic hand rub liquid

Holladay Helping Hands by

Drug Labeling and Warnings

Holladay Helping Hands by is a Otc medication manufactured, distributed, or labeled by McCormick Distilling Co., Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Front Label

HOLLADAY HELPING HANDS

ALCOHOL ANTISEPTIC 80%

TOPICAL SOLUTION

ANTISEPTIC HAND RUB NON-STERILE SOLUTION

WITH GRATITUDE TO OUR

HEALTH CARE PROFESSIONALS

PRODUCED BY HOLLADAY DISITLLING COMPANY

WESTON, MO 1.75L

Back Label

Active Ingredients

Active Ingredient(s)

Alcohol 80% v/v

Purpose

Antiseptic

Use(s)

Use(s)

Health care personnel had rub to help reduce bacteria that potentially can casue diesease.

Do not use

Do not use

• in children less than 2 months of age
• on open skin wounds

When using this product

When using this product keep out of eyes, ears, and mouth.
In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

Stop use and ask a doctor if irritations or rash occurs.
These may be signs of serous condition.

Keep out of reach of children

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

or contact a Poison Control Center right away.

Warnings

Warnings

For external use only. Flammable. Keep away from heat or flame

Directions

Directions

• Place enough product on hands to cover all surfaces.
  Rub hands together until dry.
• Supervise children under 6 years of age when using this
  product to avoid swallowing.

Other information

Other information

• Store between 1-=30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

Inactive ingredients glycerin, hydrogen peroxide, purified water USP

INGREDIENTS AND APPEARANCE

HOLLADAY HELPING HANDS 
antiseptic hand rub liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58006-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58006-001-17	1750 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/26/2020

Labeler - McCormick Distilling Co., Inc. (007138191)

Registrant - McCormick Distilling Co., Inc. (007138191)

Establishment
Name	Address	ID/FEI	Business Operations
McCormick Distilling Co., Inc.		007138191	manufacture(58006-001)