Cand-ex Liquid
FDA Label NDC 61657-0101

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by White Manufacturing Inc. Dba Micro West for the product Cand-ex (NDC 61657-0101). 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, inactive ingredients, purpose, keep out of reach of children, indications, warning, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

Asafoetida 12X

Baptisia 3X

Borax 12X

Calc carb 12X

Echinacea 3X

Gentiana lut 3X

Kreosotum 12X

Lycopodium 30X

Nux mosch 12X

Nux vom 12X

Phosphoricum ac 12X

Pulsatilla 30X

Sepia 30X

Inactive Ingredients

Inactive ingredients: Alcohol (20% v/v), Purified water

Purpose

FOR THE TEMPORARY RELIEF OF FLATULENCE, DROWSINESS, CONFUSION, VERITGO, HEADACHE, NAUSEA, AND VAGINAL DISCHARGE

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Indications

INDICATIONS: FOR THE TEMPORARY RELIEF OF FLATULENCE, DROWSINESS, CONFUSION, VERITGO, HEADACHE, NAUSEA, AND VAGINAL DISCHARGE

Warning

WARNINGS: Stop use and call a doctor if symptoms persist or worsen. If pregnant or breast-feeding, consult a healthcare professional before use. Contains alcohol; in case of accidental overdose, consult a poison control center immediately.

Directions

DIRECTIONS:Take 6 drops orally, 4 times a day. For ages 2 to adult

Other Information

Other information: Tamper resistant for your protection. Use only if safety seal is intact

Manufacture

MANUFACTURED FOR:

MICRO WEST

P.O. Box 950

DOUGLAS, WY 82633
1-307-358-5066

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