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NDC 74111-0101-55 Hand Sanitizer 80 mL/100mL Details

Hand Sanitizer 80 mL/100mL

Hand Sanitizer is a TOPICAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Hobo Inc. The primary component is ALCOHOL.

Product Information

NDC	74111-0101
Product ID	74111-101_d5cc071c-2253-c643-e053-2995a90a60e6
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Hand Sanitizer
Proprietary Name Suffix	n/a
Non-Proprietary Name	ALCOHOL
Product Type	HUMAN OTC DRUG
Dosage Form	LIQUID
Route	TOPICAL
Active Ingredient Strength	80
Active Ingredient Units	mL/100mL
Substance Name	ALCOHOL
Labeler Name	Hobo Inc
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH NOT FINAL
Application Number	part333A
Listing Certified Through	2023-12-31

Package

Package Images

NDC 74111-0101-55 (74111010155)

Pricing Information	N/A
NDC Package Code	74111-101-55
Billing NDC	74111010155
Package	208175 mL in 1 DRUM (74111-101-55)
Marketing Start Date	2020-05-01
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL a49d0ad5-02a1-1782-e053-2995a90a5043 Details

SPL UNCLASSIFIED SECTION

The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation):

Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (80%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
Glycerol (1.45% v/v).
Hydrogen peroxide (0.125% v/v).
Fragrance (0.200% v/v)
Sterile distilled water or boiled cold water.

Active Ingredient(s)

Alcohol 80% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

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

Do not use

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

SPL UNCLASSIFIED SECTION

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 if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

SPL UNCLASSIFIED SECTION

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

SPL UNCLASSIFIED SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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

Store between 15-30C (59-86F)
Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

glycerin, hydrogen peroxide, fragrance, purified water USP

Package Label - Principal Display Panel

30 mL NDC: 74111-101-30

60 mL NDC: 74111-101-60

480 mL NDC: 74111-101-16

960 mL NDC: 74111-101-32

3785 mL NDC: 74111-101-01

9460 mL NDC: 74111-101-25

18925 mL NDC: 74111-101-05

208175 mL NDC: 74111-101-55

INGREDIENTS AND APPEARANCE

HAND SANITIZER

alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:74111-101
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
GLYCERIN (UNII: PDC6A3C0OX)	1.45 mL in 100 mL
HYDROGEN PEROXIDE (UNII: BBX060AN9V)	0.125 mL in 100 mL
WATER (UNII: 059QF0KO0R)
CINNAMALDEHYDE (UNII: SR60A3XG0F)	0.01 mL in 100 mL
ISOAMYL ACETATE (UNII: Z135787824)	0.005 mL in 100 mL
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)	0.01 mL in 100 mL
HEXAMETHYLINDANOPYRAN (UNII: 14170060AT)	0.175 mL in 100 mL

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:74111-101-01	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
2	NDC:74111-101-16	480 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
3	NDC:74111-101-32	960 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
4	NDC:74111-101-30	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
5	NDC:74111-101-60	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
6	NDC:74111-101-25	9460 mL in 1 JUG; Type 0: Not a Combination Product	05/01/2020
7	NDC:74111-101-05	18925 mL in 1 PAIL; Type 0: Not a Combination Product	05/01/2020
8	NDC:74111-101-55	208175 mL in 1 DRUM; Type 0: Not a Combination Product	05/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	05/01/2020

Labeler - Hobo Inc (944358548)

Name	Address	ID/FEI	Business Operations
Establishment
Hobo Inc		944358548	manufacture(74111-101)

Revised: 1/2022

Document Id: d5cc071c-2253-c643-e053-2995a90a60e6

Set id: a49d0ad5-02a1-1782-e053-2995a90a5043

Version: 2

Effective Time: 20220117

Search by Drug Name or NDC

NDC 74111-0101-55 Hand Sanitizer 80 mL/100mL Details

Hand Sanitizer 80 mL/100mL

Product Information

Package

Package Images

NDC 74111-0101-55 (74111010155)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL a49d0ad5-02a1-1782-e053-2995a90a5043 Details

SPL UNCLASSIFIED SECTION

Active Ingredient(s)

Purpose

Use

Warnings

Do not use

SPL UNCLASSIFIED SECTION

SPL UNCLASSIFIED SECTION

SPL UNCLASSIFIED SECTION

Directions

Other information

Inactive ingredients

Package Label - Principal Display Panel

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