Alcohol Prep Pad
FDA Label NDC 58488-004

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Tongzhou Ruihong Medical Products Factory for the product Alcohol Prep Pad (NDC 58488-004). 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 ingredient, purpose, use, warnning, otc - keep out of reach of children, directions, inactive ingredients, 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

Active Ingredient

Isopropyl Alcohol 70%

Purpose

Antiseptic

Use

For preparation of skin prior to injection prior to injection and to decrease germs in minor cuts and scrapes,

Warnning

For External use only.

Stop use and ask a doctor if irritation develops.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children  except with adult supervision.

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

Directions

Apply topically as needed to cleanse intended area.

Discard after single use.

Inactive Ingredients

Inactive Ingredients: Water

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