Bactoflam Liquid
FDA Label NDC 61657-0052

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 Bactoflam (NDC 61657-0052). 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 ingredient, purpose, keep out of reach of children, warnings, indications, directions, manufacture, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

Apis mel 12X

Arsenicum alb 12X

Baptisia 3X

Belladonna 12X

Echinacea 3X

Ferrum phos 12X

Rhus tox 12X

Inactive Ingredient

Alcohol (20% v/v, Purified water

Purpose

TEMPORARY RELIEF OF HEAT, REDNESS, SWELLING DUE TO INFLAMMATION

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Warnings

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

Indications

FOR THE TEMPORARY RELIEF OF HEAT, REDNESS, SWELLING DUE TO INFLAMMATION

Directions

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

Manufacture

MANUFACTURED FOR MICRO WEST

DOUGLAS, WY 82633

1-307-358-5066

Other Information

Tamper resistant for you protection; use only if safety seal is intact

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