Gaffer and Child Hand Sanitizer

Manufacturer: Gaffer and Child, LLC
Effective date: 2020-10-08
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:31:18

Label at a glance#

ProductGaffer and Child Hand Sanitizer

Active ingredientALCOHOL

Label structure8 sections

Dosage and administration

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.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

USE(S)

INDICATIONS & USAGE SECTION

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

WARNINGS

WARNINGS SECTION

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

DO NOT USE

OTC - DO NOT USE SECTION

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

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly

STOP USE AND ASK A DOCTOR

OTC - STOP USE SECTION

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

KEEP OUT OF REACH OF CHILDREN.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

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

SPL UNCLASSIFIED SECTION

Store at 15°-30°C (59°-86°F)
Avoid freezing / excessive heat above 40C (104F)

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

golden lemon essential oil, vegetable glycerin, purified water

QUESTIONS?

OTC - QUESTIONS SECTION

hello@gafferandchild.com

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
582753	ethanol 70 % Topical Solution	PSN	1
582753	ethanol 0.7 ML/ML Topical Solution	SCD	1
582753	ethanol 70 % Topical Solution	SY	1
582753	ethyl alcohol 70 % Topical Solution	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
80634-002-01	2022-01-28	C162847	48780-1	d6a99b39-b1a1-a426-e053-dadaa90af4c2	Gaffer and Child Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
80634-002-01	Gaffer and Child Hand Sanitizer	3780 mL in 1 JUG	LIQUID	3780		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
80634-002	GAFFER AND CHILD HAND SANITIZER (ALCOHOL) LIQUID [GAFFER AND CHILD, LLC]	1	Legacy NDC, 1 package rows	20201009_b12c22cf-f86a-0c53-e053-2995a90a34c7.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

Gaffer and Child Hand Sanitizer
ALCOHOL
GLYCERIN
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
80634-002	80634-002-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
b12bf3ea-c5e3-71ab-e053-2995a90accc0			b12c22cf-f86a-0c53-e053-2995a90a34c7	2020-10-08	Warnings	Exact identifier spl id: b12bf3ea-c5e3-71ab-e053-2995a90accc0 spl set id: b12c22cf-f86a-0c53-e053-2995a90a34c7

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.