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OINTMENT

FDA Drug Reference

Dermedial Anti-Ouch

Generic: Menthol

Dosage Form

OINTMENT

Route

TOPICAL

NDC

69204-029

This page summarizes official FDA drug label records for professional reference. Verify prescribing decisions against the complete current label and institutional policy.

Label Record Status

Data from U.S. Food and Drug Administration label records. Listing expiration: Date unavailable

Clinical Pharmacology

Indications & Usage

Dermedial Anti-Ouch is listed as a OINTMENT formulation in the OINTMENT category. Consult official FDA labeling for full prescribing information.

Administration Context

Dermedial Anti-Ouch is administered via the TOPICAL route as a OINTMENT.

Administration Protocol

Prescribing Information

Refer to official FDA labeling or institutional protocols for complete dosage and administration instructions.

Safety Profile

Contraindications & Warnings

Consult the official FDA-approved labeling for complete contraindications, warnings, precautions, and patient-specific safety information.

National Drug Registry

Product and label metadata.

Marketing Category

OTC MONOGRAPH DRUG

Route of Administration

TOPICAL

National Drug Code

69204-029

Manufacturer / Labeler

Natures Formulae Health Products Ltd.

Dosage Form

OINTMENT

Strength

See labeling

Application Number

M017

SPL Identifier

3ce290d6-8818-87a4-e063-6294a90a74d2

WHO Regulatory Intelligence

Vaccine Safety Information

Access evidence-based safety data and clinical guidelines from global health resources.

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