Cabana Bay Beach Resort Hand Sanitizer Gel
FDA Label NDC 78828-113

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Carretta Usa, Inc for the product Cabana Bay Beach Resort Hand Sanitizer Gel (NDC 78828-113). 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, use[s], 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

Use[S]

Hand sanitizer to help reduce bacteria that potentially can cause disease.

For use when soap and water are not available.

Warnings

For external use only.Flammable.

Keep away from heat or flame.

Do not use

  • in children less than 2 months of age
  • on open skin wounds

    • When using this product keep out of eyes, ears,and mouth. In case of contact with eyes,rinse eyes thoroughly with water.

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep Out Of Reach Of Children.

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

Directions

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

  • Store between 15-30C (59-83F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive Ingredients:

Water,Glycerin,Propylene glycol,Carbomer,Aloe Vera Extract,Triethanolamine,Disodium Edta

Packaging

Image (Cabana1)

Image (Cabana1)

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