Active Ingredient
​alchol70%
Bcp Hand Sanitizer
FDA Label NDC 78252-302
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Best Chance Products, Llc for the product Bcp Hand Sanitizer (NDC 78252-302). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, inactive ingredient, direction, do not use, use, warnings, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Inactive Ingredient
ALCOHOL, JOJOBA OIL, GREEN TEA LEAF
GLYCERIN, CHAMAECYPARIS LAWSONIANA WOOD OIL , CARBOMER
ALOE VERA LEAF , WATER , PROPYLENE GLYCOL ,TROLAMINE
Direction
Take an appropriate amount on your hands and rub thoroughly to dry.
for external use only
Do Not Use
around the eyes ane ears. Do not apply to broken irritated, or itching skin.Do not ingest.
Use
Hand sanitizer to help reduce bacteria that potentially can cause disease.
For use when soap and water are not avaliable.
Warnings
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.
If swallowed contact your doctor immediately
Stop Use And Ask A Doctor.
if the following symptoms appear,Stop use and immediately consult a doctor: rash, erythema, itching, edema or any other skin irritation.
Other Information
keep container upright. Store at room temperature (1-30'C)
Indication
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
78252-302-01
78252-302-01 (3800ml)
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