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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

Source: 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

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