Happ Hand Sanitizer

Manufacturer: Fujian Happiness Biotech Technology Co., Ltd.
Effective date: 2020-07-02
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:21:18

Label at a glance#

ProductHapp Hand Sanitizer

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

to decrease bacteria on the skin that could cause disease recommended for repeated use

Dosage and administration

Wet hand thoroughly and allow to dry without wiping For children under 6, use only under adult supervision not recommended for infants

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 65% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin that could cause disease
recommended for repeated use

Warnings

WARNINGS SECTION

For external use only - hands

Flammable, keep away from heat and flame

When using the product

keep out of eyes, in case of contact with eyes, flush thoroughly with water
avoid contact with broken skin
do not inhale or ingest

Stop use and ask a doctor if skin irritation develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hand thoroughly and allow to dry without wiping
For children under 6, use only under adult supervision
not recommended for infants

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water, Glycerin, Polyacrylic acid, Aminomethylpropanol

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
902574	ethanol 65 % Topical Gel	PSN	1
902574	ethanol 0.65 ML/ML Topical Gel	SCD	1
902574	ethyl alcohol 65 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76735-001-01	2022-01-28	C162847	48780-1	d6a99b39-5cb9-a426-e053-dadaa90af4c2	99611b02-b058-4c07-8800-5b76bc854850
76735-001-02	2022-01-28	C162847	48780-1	d6a99b39-5cb9-a426-e053-dadaa90af4c2	99611b02-b058-4c07-8800-5b76bc854850
76735-001-03	2022-01-28	C162847	48780-1	d6a99b39-5cb9-a426-e053-dadaa90af4c2	99611b02-b058-4c07-8800-5b76bc854850
76735-001-04	2022-01-28	C162847	48780-1	d6a99b39-5cb9-a426-e053-dadaa90af4c2	99611b02-b058-4c07-8800-5b76bc854850

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
76735-001-01	Happ Hand Sanitizer	50 mL in 1 BOTTLE, PLASTIC	GEL	50	1
76735-001-02	Happ Hand Sanitizer	100 mL in 1 BOTTLE, PLASTIC	GEL	100	1
76735-001-03	Happ Hand Sanitizer	236 mL in 1 BOTTLE, PLASTIC	GEL	236	1
76735-001-04	Happ Hand Sanitizer	500 mL in 1 BOTTLE, PLASTIC	GEL	500	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76735-001	HAPP HAND SANITIZER (ALCOHOL) GEL [FUJIAN HAPPINESS BIOTECH TECHNOLOGY CO., LTD.]	1	Legacy NDC, 4 package rows	20200715_99611b02-b058-4c07-8800-5b76bc854850.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Happ Hand Sanitizer
Alcohol
GLYCERIN
POLYACRYLIC ACID (250000 MW)
WATER
AMINOMETHYLPROPANOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76735-001	76735-001-01, 76735-001-02, 76735-001-03, 76735-001-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
GLYCERIN	PDC6A3C0OX	IACT
POLYACRYLIC ACID (250000 MW)	9G2MAD7J6W	IACT
WATER	059QF0KO0R	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT

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
865d093f-87db-46b5-aecf-6b2d5b5244a7			99611b02-b058-4c07-8800-5b76bc854850	2020-07-02	Warnings	Exact identifier spl id: 865d093f-87db-46b5-aecf-6b2d5b5244a7 spl set id: 99611b02-b058-4c07-8800-5b76bc854850

Reported adverse events (FAERS/openFDA)#

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