BCP HAND SANITIZER

Manufacturer
Best Chance Products, LLC | ECOSEM Co.,Ltd.
Effective date
2020-06-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:17:48

Label at a glance#

ProductBCP HAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

​alchol70%

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

inactive ingredient

INACTIVE INGREDIENT SECTION

ALCOHOL, JOJOBA OIL, GREEN TEA LEAF
GLYCERIN, CHAMAECYPARIS LAWSONIANA WOOD OIL , CARBOMER
ALOE VERA LEAF , WATER , PROPYLENE GLYCOL ,TROLAMINE

Direction

DOSAGE & ADMINISTRATION SECTION

Take an appropriate amount on your hands and rub thoroughly to dry.

for external use only

Do not use

OTC - DO NOT USE SECTION

around the eyes ane ears. Do not apply to broken irritated, or itching skin.Do not ingest.

Use

OTC - WHEN USING SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease.
For use when soap and water are not avaliable.

Warnings

WARNINGS SECTION

for external use only.

Do not get in eyes. do not inhale vapor.

do not use under bandages, as irritation may develop.

do not use for any other purpose but hands sanitization.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed contact your doctor immediately

Stop use and ask a doctor.

OTC - STOP USE SECTION

if the following symptoms appear,Stop use and immediately consult a doctor: rash, erythema, itching, edema or any other skin irritation.

Other information

OTHER SAFETY INFORMATION

keep container upright. Store at room temperature (1-30'C)

indication

INDICATIONS & USAGE SECTION

After use, properly close the product to avoid drying out or spilling.

Take an appropriate amount on your hands and rub thoroughly to dry.

pakage label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

78252-302-01

78252-302-0178252-302-01

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78252-302-012021-07-23C16284748780-1c7ccaba7-2637-fd44-e053-dadaa90aa01bSanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78252-302-01BCP HAND SANITIZER3800 mL in 1 BOTTLE, PLASTICGEL38002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78252-302BCP HAND SANITIZER (ALCOHOL) GEL [BEST CHANCE PRODUCTS, LLC]2Legacy NDC, 1 package rows20200616_a81a51b3-fc21-87f6-e053-2a95a90ac3b5.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78252-30278252-302-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
a81a51b3-fc22-87f6-e053-2a95a90ac3b5a81a51b3-fc21-87f6-e053-2a95a90ac3b52020-06-15WarningsExact identifier
spl id: a81a51b3-fc22-87f6-e053-2a95a90ac3b5
spl set id: a81a51b3-fc21-87f6-e053-2a95a90ac3b5

Reported adverse events (FAERS/openFDA)#

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