FDA.reportPublic FDA data

BCP HAND SANITIZER

Manufacturer
Best Chance Products, LLC | ECOSEM Co.,Ltd.
Effective date
2020-06-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:17:41

Label at a glance#

ProductBCP HAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Watch for children under 6 years of age to avoid rubbing, rubbing them on their backs, or drinking this product.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ethanol alchol 65%

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Water, Glycerin, Propylene glycol, Cabomer940, Aloe Vera gel, Triethanolamine, Jojoba Oil
green tea Leaf Extract, Chamaecyparis Lawsoniana Wood Oil

USE

DOSAGE & ADMINISTRATION SECTION

Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

OTHER INFORMATION

OTHER SAFETY INFORMATION

1. Store in cool and shady place, between 15-30C (59-86F)

2. May discolor certain fabrics or surfaces.

Stop use and ask a doctor if sings symptoms as follows

OTC - STOP USE SECTION

1) signs of irritation and/or rash appears

(2) signs of abnormality as above after exposed to sunlight.

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.

Do not use

OTC - DO NOT USE SECTION

In children less than 2 months of age.
On open skin wounds

WARNING

WARNINGS SECTION

Flammable. Keep away from heat or flame. Use only as intended and according to the directions of use.

When using this product

OTC - WHEN USING SECTION

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thorough with water.

Directions

INDICATIONS & USAGE SECTION

Watch for children under 6 years of age to avoid rubbing, rubbing them on their backs, or drinking this product.

PAKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60ml 78252-301-01

78252-301-0178252-301-01

125ml 78252-301-02

78252-301-0278252-301-02

250ml 78252-301-03

78252-301-0378252-301-03500ml 78252-301-04

78252-301-0478252-301-04

1000ml 78252-301-05

78252-301-0578252-301-05

200L 78252-301-06

78252-301-0678252-301-06

1000L 78252-301-07

78252-301-0778252-301-07

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
902574ethanol 65 % Topical GelPSN1
902574ethanol 0.65 ML/ML Topical GelSCD1
902574ethyl alcohol 65 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78252-301-012021-07-23C16284748780-1c7ccaba7-1797-fd44-e053-dadaa90aa01bsanitizer
78252-301-022021-07-23C16284748780-1c7ccaba7-1797-fd44-e053-dadaa90aa01bsanitizer
78252-301-032021-07-23C16284748780-1c7ccaba7-1797-fd44-e053-dadaa90aa01bsanitizer
78252-301-042021-07-23C16284748780-1c7ccaba7-1797-fd44-e053-dadaa90aa01bsanitizer
78252-301-052021-07-23C16284748780-1c7ccaba7-1797-fd44-e053-dadaa90aa01bsanitizer
78252-301-062021-07-23C16284748780-1c7ccaba7-1797-fd44-e053-dadaa90aa01bsanitizer
78252-301-072021-07-23C16284748780-1c7ccaba7-1797-fd44-e053-dadaa90aa01bsanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78252-301-01BCP HAND SANITIZER60 mL in 1 BOTTLEGEL601
78252-301-02BCP HAND SANITIZER125 mL in 1 BOTTLEGEL1251
78252-301-03BCP HAND SANITIZER250 mL in 1 BOTTLE, PUMPGEL2501
78252-301-04BCP HAND SANITIZER500 mL in 1 BOTTLE, PUMPGEL5001
78252-301-05BCP HAND SANITIZER1000 mL in 1 BOTTLE, PUMPGEL10001
78252-301-06BCP HAND SANITIZER200000 mL in 1 DRUMGEL2000001
78252-301-07BCP HAND SANITIZER1000000 mL in 1 DRUMGEL10000001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78252-301BCP HAND SANITIZER (ALCOHOL) GEL [BEST CHANCE PRODUCTS, LLC]1Legacy NDC, 7 package rows20200615_a7e51465-f1d5-c197-e053-2995a90afef0.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
78252-30178252-301-01, 78252-301-02, 78252-301-03, 78252-301-04, 78252-301-05, 78252-301-07, 78252-301-06

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
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER 9404Q93RCW27EIACT
ALOE VERA LEAFZY81Z83H0XIACT
JOJOBA OIL724GKU717MIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
CHAMAECYPARIS LAWSONIANA WOOD OIL0H3D02DVNUIACT
GLYCERINPDC6A3C0OXIACT
TROLAMINE9O3K93S3TKIACT

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
a7e51465-f1d6-c197-e053-2995a90afef0a7e51465-f1d5-c197-e053-2995a90afef02020-06-12WarningsExact identifier
spl id: a7e51465-f1d6-c197-e053-2995a90afef0
spl set id: a7e51465-f1d5-c197-e053-2995a90afef0

Reported adverse events (FAERS/openFDA)#

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