Modaka
FDA Label NDC 77779-002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by We Labs Company Limited for the product Modaka (NDC 77779-002). 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 (s), purpose, warnings, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient (S)

Ethyl Alcohol 70% v/v

Purpose

Anti-Bacterial, Anti-microbial and Germs

Warnings

Flammable, keep away from fire and flames

For external use only

When using this product

- do not get into eyes

- if contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if

- irritation and redness develop

Packaging

Image (Labelgel)

Image (Labelgel)

* Please review the disclaimer below.