BEING WELL HAND SANITIZER 2 PACK

Manufacturer
NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.
Effective date
2021-01-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:56:46

Label at a glance#

ProductBEING WELL HAND SANITIZER 2 PACK
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

Helps reduce bacteria on the skin that could cause disease. Recommended for repeated use.

Dosage and administration

pump as needed into your palms and thoroughly spread on both hands. rub into skin until dry.

Storage and handling

store at 20℃ (68° to 77°F). may discolor fabrics.

Label contents#

Full prescribing information#

Drug Facts Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62 percent

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Helps reduce bacteria on the skin that could cause disease. Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only. Do not swallow.

Do not apply around eyes. Do not use in ears and mouth.

When using this product, avoid contact with eyes. In case of contact, flush eyes with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

redness or irritation develop and persist for more than 72 hours.

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

pump as needed into your palms and thoroughly spread on both hands. rub into skin until dry.

Other information

STORAGE AND HANDLING SECTION

store at 20℃ (68° to 77°F). may discolor fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, triethanolamine, glycerin, propylene glycol, tocopheryl acetate, aloe barbadensis gel, carbomer, fragrance.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76176-12776176-127-02, 76176-127-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
b8bf4662-f582-1321-e053-2995a90ad362b8bf4656-0071-3a1f-e053-2a95a90a2ab72021-01-01WarningsExact identifier
spl id: b8bf4662-f582-1321-e053-2995a90ad362
spl set id: b8bf4656-0071-3a1f-e053-2a95a90a2ab7

Reported adverse events (FAERS/openFDA)#

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