B.C., Hand Sanitizer, 70% Alcohol, Gel, N 236mL

Manufacturer
GuangDong B.C. Biotech Co., Ltd. | A03 Lab of BTS
Effective date
2020-05-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:10:15

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry. Children under 6 years of age should be supervised when using this product.

Storage and handling

Store below 106℉ (41℃) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v. Purpose: Antimicrobial

Purpose

OTC - PURPOSE SECTION

Hand Sanitizer to help reduce bactreia on skin.

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on skin.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only.

Do not use

OTC - DO NOT USE SECTION

Do not use in or near 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.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts.

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

  • Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry.
  • Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

  • Store below 106℉ (41℃)
  • May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Olive Oil PEG-7 Esters, Acrylates/C10-30 Alkyl, Acrylate Crosspolymer, Aminomethyl Propanol, Aloe Barbadensis Leaf Extract

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

N 236N 236

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74738-1105-72021-07-23C16284748780-1c7ccaba7-25f5-fd44-e053-dadaa90aa01bB.C., Hand Sanitizer, 70% Alcohol, Gel, N 236mL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74738-1105-2Hand Sanitizer236 mL in 1 BOTTLEGEL2361
74738-1105-7Hand Sanitizer24 in 1 CARTONGEL241

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74738-1105HAND SANITIZER (ALCOHOL) GEL [GUANGDONG B.C. BIOTECH CO., LTD.]1Legacy NDC, 2 package rows20200508_a51272c1-91fc-06aa-e053-2995a90aa3d3.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74738-110574738-1105-2, 74738-1105-7

Ingredients#

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

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

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a51272c1-91fd-06aa-e053-2995a90aa3d3a51272c1-91fc-06aa-e053-2995a90aa3d32020-05-07WarningsExact identifier
spl id: a51272c1-91fd-06aa-e053-2995a90aa3d3
spl set id: a51272c1-91fc-06aa-e053-2995a90aa3d3

Reported adverse events (FAERS/openFDA)#

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