Solgreat Instant Hand Sanitizer
FDA Label NDC 73913-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Panatural Usa, Inc. for the product Solgreat Instant Hand Sanitizer (NDC 73913-001). 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 lngredient, purpose, uses, warnings, directions, inactives, keep out of reach of children., other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Lngredient

Ethyl Alcohol

Purpose

Antiseptic 

Uses

• hand sanitizer to help decrease bacteria on the skin, when water, soap & towel are not available.
• recommended for repeated use

Warnings


For external use only.

Flammable. Keep away from fire or flame.

Do not apply around eyes. Do not use in ears & mouth.

When using this product, avoid contact with eyes. In case of contact flush eyes with water.

Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

Directions

  • place enough product into your palms and thoroughly spread on both hands.
  • rub into skin until dry.

Inactives

aloe barbadensis leaf juice, carbomer, triethanolamine, glycerin, propylene glycol, tocopheryl acetate, water.

Keep Out Of Reach Of Children.

Children must be supervised in use of this product.

Other Information

  • store below 1100F (43oC).
  • may discolor certain fabrics or surfaces.

Product Labe-60Ml Solgreat Alcohol Hand Sanitizer

60ml (22oz Alchol)

60ml (22oz Alchol)

Product Label 500Ml Solgreat Alcohol Hand Sanitizer

500ml (16.9oz)

500ml (16.9oz)

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