Spatherapy
FDA Label NDC 56136-011

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Xiamen Olivee Daily Use Chemical Co., Ltd. for the product Spatherapy (NDC 56136-011). 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 inactive ingredient, otc - active ingredient, otc - purpose, indications & usage, dosage & administration, warnings, otc - when using, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Inactive Ingredient

Inactive Ingredients - Water, Sodium Laureth

Sulfate, Cocamidopropyl Betaine, Glycerin, DMDM

Hydantoin, Benalkonium Clhoride, Fragrance,

Xanthan Gum, Disodium EDTA,

Citiric Acid. May contain: CI 14700, CI 17200, CI 19140, Ci 42090

Otc - Active Ingredient

Active Ingredient

Benzalkonium Chloride  0,2 %

Otc - Purpose

Purpose

Antibacterial

Indications & Usage

Use - handwashing to decrease bacteria on skin

Dosage & Administration

Directions - wet hands, work into

rich lather - rinse well

Warnings

Warnings

For external use only

Otc - When Using

When using this product, avoid contact with eyes. If contact occurs,

rinse thoroughly with water.

Otc - Stop Use

Stop use and ask a doctor if irritation and redness develop

Otc - Keep Out Of Reach Of Children

EKeep out of reach of children. If swallowed, get medical help

or contact a Poison Control Center right away.

Otc - Questions

Questions? 1-800-FDA-1088

Package Label.Principal Display Panel

Copy Of Label (Pumpkin Label)

Copy Of Label (Pumpkin Label)

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