Forest Fresh
FDA Label NDC 25113-222

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by The Dodge Company, Inc. for the product Forest Fresh (NDC 25113-222). 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 warnings section, otc - keep out of reach of children section, indications & usage section, otc - purpose section, dosage & administration section, otc - active ingredient section, inactive ingredient section, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Warnings Section

1) For external use only.

2) Do not use in the eyes.

3) Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a doctor.

Otc - Keep Out Of Reach Of Children Section

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Indications & Usage Section

Antiseptic handwash for handwashing to decrease baceria on the skin.

Otc - Purpose Section

Antiseptic handwash

Dosage & Administration Section

Moisten surface to be cleaned, apply soap, rub to create lather, and rinse.  Repeat as needed.

Otc - Active Ingredient Section

Triclosan

Inactive Ingredient Section

cocamidopropyl betaine

cocodiethanolamide

citric acid monohydrate

FD&C blue No.1

imidazolidinyl urea

myristamine oxide

potassium cocoate

propylene glycol

sodium C14-C16 olefin sulfonate

sodium chloride

sodium lauryl sulfate

water

Package Label.Principal Display Panel

Forest Fresh 8oz.jpg

Forest Fresh 16oz.jpg

Forest Fresh Gal.jpg

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