Hand Sanitizer

Manufacturer: M3 Group LLC | Guangzhou Berfly Cosmetic Co., Ltd
Effective date: 2020-05-27
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:14:54

Label at a glance#

ProductHand Sanitizer SAYFE

Active ingredientALCOHOL

Label structure12 sections

Dosage and administration

■ place enough product in your palm to thoroughly cover both hands ■ 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 Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

■ hand sanitizer to help reduce bacteria on the skin. 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

■ avoid getting into the eyes. ■ in case of eye contact immediately flush eyes throughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ irritation or redness develops ■ conditions persist for more than 72 hours ■ redness is present

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, contact a doctor or Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

■ place enough product in your palm to thoroughly cover both hands ■ rub hands together until dry ■ Supervise children under 6 years of age when using this product to avoid swallowing

Other information

SPL UNCLASSIFIED SECTION

■ do not store above 105ºF ■ may discolor fabrics or surfaces

Inactive Ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, carbomer, aloe extract,sodium hydroxide

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
582753	ethanol 70 % Topical Solution	PSN	2
582753	ethanol 0.7 ML/ML Topical Solution	SCD	2
582753	ethanol 70 % Topical Solution	SY	2
582753	ethyl alcohol 70 % Topical Solution	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
74176-001-02	2022-01-28	C162847	48780-1	d6a99b39-a784-a426-e053-dadaa90af4c2	Sayfe Hand Sanitizer
74176-001-08	2022-01-28	C162847	48780-1	d6a99b39-a784-a426-e053-dadaa90af4c2	Sayfe Hand Sanitizer
74176-001-16	2022-01-28	C162847	48780-1	d6a99b39-a784-a426-e053-dadaa90af4c2	Sayfe Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
74176-001-02	Hand SanitizerSAYFE	59 mL in 1 BOTTLE, PLASTIC	SOLUTION	59	2
74176-001-08	Hand SanitizerSAYFE	250 mL in 1 BOTTLE, PUMP	SOLUTION	250	2
74176-001-16	Hand SanitizerSAYFE	500 mL in 1 BOTTLE, PLASTIC	SOLUTION	500	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74176-001	HAND SANITIZER SAYFE (ALCOHOL) SOLUTION [M3 GROUP LLC]	2	Legacy NDC, 3 package rows	20200528_a40df265-6f90-3010-e053-2a95a90a32d1.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Hand Sanitizer SAYFE
Alcohol
SODIUM HYDROXIDE
GLYCERIN
ALOE VERA LEAF
WATER
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74176-001	74176-001-08, 74176-001-16, 74176-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SODIUM HYDROXIDE	55X04QC32I	IACT
GLYCERIN	PDC6A3C0OX	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT

Source Document#

Source XML · Source PDF

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
a6a8025b-d606-20ca-e053-2995a90a6f4d			a40df265-6f90-3010-e053-2a95a90a32d1	2020-05-27	Warnings	Exact identifier spl id: a6a8025b-d606-20ca-e053-2995a90a6f4d spl set id: a40df265-6f90-3010-e053-2a95a90a32d1

Reported adverse events (FAERS/openFDA)#

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