AM-9: Homeopathic Product Information

AM-9- spigelia anthelmia, silicon dioxide and corallium rubrum whole solution
DNA Labs, Inc.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

NDC 58264-0348-1

INDICATIONS

Regulates energy flow in the triplewarmer meridian.

INGREDIENTS

ACTIVE

Spigelia anthelmia 8x, Silicea 8x, Corallium rubrum 10x

INACTIVE

20% alcohol in purified water.

SUGGESTED DOSAGE

5 to 10 drops twice a day, meridian energy excess 1 to 5 drops t.i.d, meridian lacking in energy 10 to 20 drops t.i.d.

SHAKE WELL

Warnings

  • Use only if cap seal is unbroken.
  • If pregnant or breastfeeding, ask a healthcare professional before use.
  • Keep this and all medication out of the reach of children.

To be used according to standard homeopathic indications.

PRINCIPAL DISPLAY PANEL — 1 FL. OZ. Bottle Label

DYNAMIC NUTRITIONAL
ASSOCIATES, INC.

AM-9 TRIPLEWARMER

ACUPUNCTURE MERIDIAN

1 FL. OZ.

PRINCIPAL DISPLAY PANEL -- 1 FL. OZ. Bottle Label
(click image for full-size original)
AM-9
spigelia anthelmia, silicon dioxide, and corallium rubrum whole solution
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:58264-0348
Route of Administration SUBLINGUAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SPIGELIA ANTHELMIA (SPIGELIA ANTHELMIA) SPIGELIA ANTHELMIA 8 [hp_X] in 1 mL
SILICON DIOXIDE (SILICON DIOXIDE) SILICON DIOXIDE 8 [hp_X] in 1 mL
CORALLIUM RUBRUM WHOLE (CORALLIUM RUBRUM WHOLE) CORALLIUM RUBRUM WHOLE 10 [hp_X] in 1 mL
Inactive Ingredients
Ingredient Name Strength
ALCOHOL
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:58264-0348-1 29.57 mL in 1 BOTTLE, GLASS None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 01/01/1990
Labeler — DNA Labs, Inc. (031784339)

Revised: 06/2022 DNA Labs, Inc.

HomeoLabels.com provides trustworthy package insert and label information about marketed homeopathic remedies as submitted by manufacturers to the U.S. Food and Drug Administration. Package information is not reviewed or updated separately by HomeoLabels.com. Every individual package label entry contains a unique identifier which can be used to secure further details directly from the U.S. National Institutes of Health and/or the FDA.

We source our database directly from the FDA's central repository of homeopathic remedy labels and package inserts, under the Structured Product Labeling standard. Our material is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2024. All Rights Reserved.