Type 11 Dizziness Max
FDA Label NDC 50169-0006

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by T-gone Remedies for the product Type 11 Dizziness Max (NDC 50169-0006). 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 ingredients:, indications:, warnings:, keep out of reach of children:, directons:, inactive ingredients:, questions:, package label display:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients:

Belladonna 200X, Calcarea Carbonica 200C, Phosphorus 200C, Pulsatilla (Vulgaris) 200C, Silicea 200C.

Indications:

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

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

Warnings:

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

Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use if tamper evident seal is broken or missing.

Store in a cool, dry place.

Keep Out Of Reach Of Children:

Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away.

Directons:

Take two tablets twice a day under the tongue.

Inactive Ingredients:

Lactose, Mangesium stearate, Microcrystalline cellulose.

Package Label Display:

T-Gone Remedies.

Type 11 Dizziness Max

HOMEOPATHIC

120 TABLETS

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