Moxe Citrus Hand Sanitizer
FDA Label NDC 75435-813

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Be Moxe, Llc for the product Moxe Citrus Hand Sanitizer (NDC 75435-813). 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 other, active ingredient, purpose, uses, warnings, otc - do not use, stop use and ask a doctor, otc - 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

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Drug Facts

Distributed by:
Be MOXĒ LLC 4700 140th Ave N., Ste 112,
Clearwater, FL 33762

Active Ingredient

Ethyl Alcohol 70% by volume

Purpose

Antiseptic

Uses

Use to help reduce bacteria on the skin.

Warnings

  • For external use only.
  • Flammable.
  • Keep away from fire or flame.

Otc - Do Not Use

Do Not Use Near Eyes.

In case of contact, rinse eyes thoroughly with water.

Stop Use And Ask A Doctor

If skin irritation develops

Otc - 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

  • Place sanitizer on palm, rub hands together.
  • Supervise children under 6.

Other Information

Do not store over 110° F

Questions?

Call 1-800-296-3160

Inactive Ingredients

Water, Carbomer, Glycerin, Aloe Leaf Juice, Tocopheryl Acetate, Fragrance

Principal Display Panel - 118 Ml Bottle Label

MOXĒ

CITRUS

HAND
SANITIZER

70% Alcohol

MADE IN
USA

4FL OZ | 118ml

Principal Display Panel (118 ml Bottle Label)

Principal Display Panel (118 ml Bottle Label)

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