Drugplain

SnugZ Hand Sanitizer Gel 70 mL/100mL

Hand Sanitizer Gel · GEL · SnugZ/USA, LLC

No Recall History
Plain English

SnugZ Hand Sanitizer Gel is a gel containing hand sanitizer gel at 70 mL/100mL, taken topical. Manufactured by SnugZ/USA, LLC.

Key Facts

Brand Name
SnugZ Hand Sanitizer Gel
Generic Name
Hand Sanitizer Gel
NDC Code (Product)
76309-301
Manufacturer
SnugZ/USA, LLC
Strength
70 mL/100mL
Dosage Form
GEL
Route
TOPICAL
Marketing Status
Application #
M003
Marketing Start
01/01/2018

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

dizziness1 reports
erythema1 reports
nausea1 reports
product odour abnormal1 reports
product use complaint1 reports
unevaluable event1 reports
urticaria1 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Indications: Helps reduce bacteria on skin.

Dosage & Administration

Wet hands thoroughly with product and rub into skin until dry.

Warnings

Warnings: For external use only. Flammable, keep away from fire. Do not use on damaged or broken skin. Keep out of eyes . Rinse with water to remove. Stop use and ask a doctor if rash occurs. Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Frequently Asked Questions

What is SnugZ Hand Sanitizer Gel used for?

SnugZ Hand Sanitizer Gel contains Hand Sanitizer Gel. It is a gel taken topical. Consult your doctor for specific uses.

Is SnugZ Hand Sanitizer Gel a controlled substance?

SnugZ Hand Sanitizer Gel is not classified as a controlled substance by the DEA.

What is the generic name for SnugZ Hand Sanitizer Gel?

The generic name for SnugZ Hand Sanitizer Gel is Hand Sanitizer Gel. There are 1 other brand versions of Hand Sanitizer Gel.

What is the NDC code for SnugZ Hand Sanitizer Gel 70 mL/100mL?

The NDC (National Drug Code) for SnugZ Hand Sanitizer Gel 70 mL/100mL is 76309-301, listed by SnugZ/USA, LLC.

Product NDC

76309-301

Package NDC

76309-301-01

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)