Vanilla Cupcake Anti Bacterial Foaming Hand
FDA Label NDC 59021-005

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Five Below for the product Vanilla Cupcake Anti Bacterial Foaming Hand (NDC 59021-005). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - ask doctor, otc - keep out of reach of children, dosage & administration, storage and handling, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active Ingredient

Triclsan 0.3%

Otc - Purpose

Purpose

Antiseptic

Indications & Usage

Uses

To decrease bacteria on the skin

Warnings

For external use only

When using this product: Keep out of eyes. Do not ingest.


Otc - Ask Doctor

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 assistance.

Dosage & Administration

Directions

  • Rub a dime size drop into hands

Storage And Handling

Other Information:

  • Do not store above 105F
  • May discolor some fabrics

Inactive Ingredient

Inactive Ingredient:

Deionized Water, Sodium Laurel Sulfate, Cocamide MEA, Fragrance, Citric Acid, Disodium EDTA, Methylisothiazolinone, Methylchloroisothiazolinone, may contain D and C Red No. 33, FD and C Red No. 40, FD and C Blue No. 1, FD and C Yellow No. 5, FD and C Yellow No. 6.

Package Label.Principal Display Panel

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Label (105)

Label (105)

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