Otc - Active Ingredient
ACONITUM NAPELLUS 3X HPUS
BRYONIA CRETICA 3X HPUS
Ab Liquid
FDA Label NDC 60986-2040
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Marco Pharma International Llc for the product Ab (NDC 60986-2040). 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, inactive ingredient, otc - purpose, otc - keep out of reach of children, otc - pregnancy or breast feeding, warnings, indications & usage, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
ETHYL ALCOHOL 20% V/V
WATER
Otc - Purpose
FOR TEMPORARY RELIEF OF MINOR INFLAMMATION AND TRAUMA
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN
Otc - Pregnancy Or Breast Feeding
IF PREGNANT OR BREAST-FEEDING, CONSULT A HEALTH PROFESSIONAL BEFORE USE
Warnings
IF SYMPTOMS PERSIST MORE THAN A FEW DAYS, CONTACT LICENSED PRACTIONER.
Indications & Usage
FOR TEMPORARY RELIEF OF MINOR INFLAMMATION AND TRAUMA
Dosage & Administration
DAY 1; TAKE 5 DROPS ON THE TONGUE EVERY 15 MINUTES FOR 2 HOURS. THEN TAKE 5 DROPS ONCE EVERY HOUR. DAY 2; TAKE 5 DROPS ONCE EVERY HOUR. DAY 3; TAKE 5 DROPS EVERY TWO HOURS. CONTINUE WITH 10 DROPS THREE TIMES DAILY
Package Label.Principal Display Panel
N11_60986-2040 (N11 60986 2040)
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