Jojo Siwa Hand Sanitizer 0.84 Oz
FDA Label NDC 70108-044

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ashtel Studios, Inc for the product Jojo Siwa Hand Sanitizer 0.84 Oz (NDC 70108-044). 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 ingredients, purposes, 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.

Drug Facts

Active Ingredients

Ethyl Alcohol 62%

Purposes

Antimicrobial

Uses

To help reduce bacteria and germs on the skin.

Warnings

Flammable. Keep away from fire or flame.

For external use only: hands

When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts.

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Put a thumbnail size amount in your palm and rub your hands together briskly until dry.
  • Children under 6 years of age should be supervised when using this product.

Other Information

▪ Store below 110°F (43°C).

▪ May discolor certain fabrics or surfaces.

▪ Harmful to wood finishes and plastics.

Inactive Ingredients

Water, Glycerin, Carbomer, Green-Tea extract, Mugwort extract, Sponge Cucumber Gourd extract, L-menthol, Triethanolamine

Packaging

Jojosiwi (Jojosi1)

Jojosiwi (Jojosi1)

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