WID, Hand Sanitizer, 70% Alcohol, Gel, 60mL

Manufacturer: WID Cosmetics (Shanghai) Co., Ltd. | A03 Lab of BTS
Effective date: 2020-04-27
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:08:21

Label at a glance#

ProductallpeaU Pure Hand Sanitizer

Active ingredientALCOHOL

Label structure12 sections

Dosage and administration

Take proper amount of product into the palm and rub hands together until dry. Supervise children under 6 years in the use of the product. Not recommended for infants.

Storage and handling

Store below 110℉ (43℃). May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Hand Sanitizer

Purpose

OTC - PURPOSE SECTION

Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to decrease on hands.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes.

In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develops and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Take proper amount of product into the palm and rub hands together until dry.
Supervise children under 6 years in the use of the product. Not recommended for infants.

Other information

STORAGE AND HANDLING SECTION

Store below 110℉ (43℃).

May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, acrylates/vinyl isodecanoate crosspolymer, propylene glycol, triethanolamine, aloe barbadensis extract, cucumis sativus extract, houttuynia cordata extract, parfum, CI 42090, CI 19140

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	1
581662	ethanol 0.7 ML/ML Topical Gel	SCD	1
581662	ethanol 70 % Topical Gel	SY	1
581662	ethyl alcohol 70 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75567-1011-1	2022-01-28	C162847	48780-1	d6a99b39-a4e6-a426-e053-dadaa90af4c2	WID, Hand Sanitizer, 70% Alcohol, Gel, 60mL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75567-1011-1	allpeaU Pure Hand Sanitizer	60 mL in 1 BOTTLE	GEL	60		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75567-1011	ALLPEAU PURE HAND SANITIZER (ALCOHOL HAND SANITIZER) GEL [WID COSMETICS (SHANGHAI) CO., LTD.]	1	Legacy NDC, 1 package rows	20200428_a44bf81a-0a0e-7323-e053-2a95a90ac819.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

allpeaU Pure Hand Sanitizer
Alcohol Hand Sanitizer
HOUTTUYNIA CORDATA FLOWERING TOP
FD&C BLUE NO. 1
CUCUMBER
TROLAMINE
WATER
ALCOHOL
PROPYLENE GLYCOL
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW)
ALOE VERA LEAF
FD&C YELLOW NO. 5

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75567-1011	75567-1011-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
HOUTTUYNIA CORDATA FLOWERING TOP	RH041UUZ22	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
CUCUMBER	YY7C30VXJT	IACT
TROLAMINE	9O3K93S3TK	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
PROPYLENE GLYCOL	6DC9Q167V3	IACT
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW)	JZ1374NL9E	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
FD&C YELLOW NO. 5	I753WB2F1M	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
a44bf81a-0a0f-7323-e053-2a95a90ac819			a44bf81a-0a0e-7323-e053-2a95a90ac819	2020-04-27	Warnings	Exact identifier spl id: a44bf81a-0a0f-7323-e053-2a95a90ac819 spl set id: a44bf81a-0a0e-7323-e053-2a95a90ac819

Reported adverse events (FAERS/openFDA)#

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