Type 11 Dizziness Max
FDA Label NDC 57520-0432

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Apotheca Company for the product Type 11 Dizziness Max (NDC 57520-0432). 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 otc - active ingredient, otc - purpose, warnings, dosage & administration, inactive ingredient, otc - questions, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

ACTIVE INGREDIENTS:  Belladonna 200C, Calcarea carbonica 200C, Phosphorus 200C, Pulsatilla 200C, Silicea 200C.

Otc - Purpose

INDICATIONS:  For relief of ringing in the ear from Dizziness, Loss of Balance.

Warnings

WARNINGS:  If pregnant or breast-feeding, ask a health professional before use.

Dosage & Administration

DIRECTIONS:  Take two tablets twice a day under the tongue.


Inactive Ingredient

INACTIVE INGREDIENTS:  Lactose, Magnesium stearate, Microcrystalline cellulose.

Otc - Questions


Manufactured for:

T-Gone Remedies

375 N. Stephanie St., Ste 1411

Henderson, NV 89014-8909

Web:  www.t-gone.com

Tel:  800-314-2910

[email protected]

Package Label.Principal Display Panel

T-Gone Remedies.

Type 11 Dizziness Max

HOMEOPATHIC

120 TABLETS

Type 11 Dizziness Max (Mm1)

Type 11 Dizziness Max (Mm1)

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