DETOX LYMPH- arsenic trioxide, clematis recta flowering top, conium maculatum flowering top, lachesis muta venom, mercuric iodide, phytolacca americana root, toxicodendron pubescens leaf, scrophularia nodosa and sulfur liquid 
Hevert Pharmaceuticals, 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.

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Detox Lymph

Drug Facts

Active ingredientsPurpose
*
Relief of discomfort associated with lymphatic swelling and edema
Arsenicum album 6X*
Clematis 4X*
Conium 6X*
Lachesis 8X*
Mercurius bijodatus 8X*
Phytolacca 4X*
Rhus toxicodendron 6X*
Scrophularia nodosa 3X*
Sulfur 4X*

Uses

For temporary relief of discomfort associated with lymphatic swelling and edema.

These statements have not been evaluated by the Food and Drug Administration. They are supported by traditional homeopathic principles.

Warnings

For oral use only.

Chronically enlarged lymph nodes can be the sign of different diseases. Therefore, consult a doctor in order to clarify the underlying disease before using this medicine. Also consult a doctor promptly in case of acute signs of inflammation (redness, heat, swelling, pain and dysfunction) and fever or enlargement of the lymph nodes during treatment.

Do not use if

  • you are allergic to Rhus toxicodendron or other plants from the cashew family

Stop use and ask a doctor if you suffer from thyroid disease or symptoms persist for more than 7 days, worsen or new symptoms occur.

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

Keep this and all medicines out of reach of children.

In case of accidental overdose, seek professional assistance or contact a poison control center immediately.

Directions

  • Adults and children over 12 years of age: Take 20 drops in water 3 times daily.
  • Consult a physician for use in children under 12 years of age.
  • Do not use for children under 1 year of age.

Other information

  • Store at 68 to 77 °F.
  • Tamper Evident: Do not use if tamper evident strip is broken or missing from base of bottle cap.
  • To report serious adverse events, call 1-855-387-6466.

Inactive ingredients

46 % ethanol V/V, purified water

Questions?

1-855-387-6466

Distributed by:
Hevert Pharmaceuticals, LLC
Eugene, OR 97401

PRINCIPAL DISPLAY PANEL - 50 ml Bottle Carton

NDC 54532-0021-5

HEVERT®
DETOX
LYMPH

Homeopathic Medicine

For the lymphatic
system

1.7 fl oz (50 ml)
46 % alcohol V/V
Oral drops

hEVERT

Principal Display Panel - 50 ml Bottle Carton
DETOX LYMPH 
arsenic trioxide, clematis recta flowering top, conium maculatum flowering top, lachesis muta venom, mercuric iodide, phytolacca americana root, toxicodendron pubescens leaf, scrophularia nodosa, and sulfur liquid
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:54532-0021
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Arsenic Trioxide (Arsenic Cation (3+)) Arsenic Trioxide6 [hp_C]  in 50 mL
Clematis Recta Flowering top (Clematis Recta Flowering top) Clematis Recta Flowering top4 [hp_C]  in 50 mL
Conium Maculatum Flowering Top (Conium Maculatum Flowering Top) Conium Maculatum Flowering Top6 [hp_C]  in 50 mL
Lachesis Muta Venom (Lachesis Muta Venom) Lachesis Muta Venom8 [hp_C]  in 50 mL
Mercuric Iodide (Mercuric Iodide) Mercuric Iodide8 [hp_C]  in 50 mL
Phytolacca Americana Root (Phytolacca Americana Root) Phytolacca Americana Root4 [hp_C]  in 50 mL
Toxicodendron Pubescens Leaf (Toxicodendron Pubescens Leaf) Toxicodendron Pubescens Leaf6 [hp_C]  in 50 mL
Scrophularia Nodosa (Scrophularia Nodosa) Scrophularia Nodosa3 [hp_C]  in 50 mL
Sulfur (Sulfur) Sulfur4 [hp_C]  in 50 mL
Inactive Ingredients
Ingredient NameStrength
Alcohol 
Water 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54532-0021-51 in 1 CARTON
150 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
UNAPPROVED HOMEOPATHIC08/01/2014
Labeler - Hevert Pharmaceuticals, Inc. (078647622)
Registrant - Hevert-Arzneimittel GmbH & Co. KG (318100617)
Establishment
NameAddressID/FEIBusiness Operations
Hevert-Arzneimittel GmbH & Co. KG318100617MANUFACTURE(54532-0021)

Revised: 8/2014
Document Id: e9cec512-4c9f-4056-b16c-ecad1e3245d1
Set id: bfdb7aaf-d4f6-4498-b02e-d9cd500c9f4e
Version: 1
Effective Time: 20140807
 
Hevert Pharmaceuticals, Inc.