Hand Sanitizer
FDA Label NDC 50049-002

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Quanzhou Besthope Household Products Co., Ltd. for the product Hand Sanitizer (NDC 50049-002). 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 drug facts, active ingredient, purpose, uses, warnings, keep out of reach of children., directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient

Ethyl Alcohol 75% v/v

Purpose

Antiseptic

Uses

To reduce bacteria that potentially can cause disease.

Warnings

For external use only
Flammable. Keep away from fire or flame
Keep out of reach of children. If swallowed, get medical help or contact a
Poison Control Center right away
When using this product
■Keep out of eyes. In case of contact with eyes, flush thoroughly with water
■Avoid contact with open skin
H Do not inhale or ingest
Stop use and ask a doctor
If skin irritation or redness develops

Keep Out Of Reach Of Children.

Keep out of reach of children. If swallowed, get medical help or contact a
Poison Control Center right away

Directions

■Wet hands thoroughly with product and allow to dry without wiping
■Children under 6 years of age use only under adult supervision
■Not recommended for infants

Other Information

1 Do not store above 105°F
1 May discolor some fabrics

Inactive Ingredients

Alcohol, Water (Aqua), Acrylates Copolymer, Xanthan Gum, Butylene
Glycol, Aminomethyl Propanol, Aloe Barbadensis Leaf Extract

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