Lymphdrainex
- Manufacturer
- Apotheca Company
- Effective date
- 2022-04-06
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:04:04
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
ACTIVE INGREDIENTS: Geranium robertianum 3X, 4X, Nasturtium aquaticum 3X, 4X, Aloe socotrina 3X, 4X, 6X, 8X, 12X, Juglans regia 3X, 6X, Myosotis arvensis 3X, 6X, Scrophularia nodosa 3X, 6X, Teucrium scorodonia 3X, 6X, Apis mellifica 4X, Equisetum hyemale 4X, Fumaria officinalis 4X, Natrum sulphuricum 4X, Phytolacca decandra 4X, Pinus sylvestris 4X, Veronica officinalis 4X, Gentiana lutea 5X, Sarsaparilla 6X, Baryta carbonica 8X, Hepar sulphuris calcareum 8X, Mercurius cyanatus 8X, Ferrum iodatum 8X, 12X, Aranea diadema 12X, Calcarea phosphorica 12X, Glandula parathyroidea 12X, Glandula thymi 12X, Thyroidinum 12X.
OTC - PURPOSE SECTION
INDICATIONS: For temporary relief of symptoms of acute or chronic lymphatic congestion; general immune support and lymphatic drainage.
WARNINGS SECTION
WARNINGS: If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.
DOSAGE & ADMINISTRATION SECTION
SUGGESTED USE: Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional. Consult a physician for use in children under 12 years of age.
INACTIVE INGREDIENT SECTION
INACTIVE INGREDIENTS: Demineralized water, 20% Ethanol.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center right away.
INDICATIONS & USAGE SECTION
INDICATIONS: For temporary relief of symptoms of acute or chronic lymphatic congestion; general immune support and lymphatic drainage.
OTC - QUESTIONS SECTION
Dist. by Energique, Inc.
201 Apple Blvd.
Woodbine, IA 51579
800-869-8078
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
ENERGIQUE
LYMPHDRAINEX
Homeopathic Remedy
1 fl. oz. (30 ml)
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 57520-0596-1 | 2022-04-08 | C162847 | 48780-1 | 9d75b9d0-daf2-f424-e053-dadaa90a57ce | Lymphdrainex |
| 57520-0596-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-daf2-f424-e053-dadaa90a57ce | Lymphdrainex |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| ALOE | ACTIVE INGREDIENT | V5VD430YW9 | 1 | |
| APIS MELLIFERA | ACTIVE INGREDIENT | 7S82P3R43Z | 1 | |
| ARANEUS DIADEMATUS | ACTIVE INGREDIENT | 6T6CO7R3Z5 | 1 | |
| BARIUM CARBONATE | ACTIVE INGREDIENT | 6P669D8HQ8 | 1 | |
| CALCIUM SULFIDE | ACTIVE INGREDIENT | 1MBW07J51Q | 1 | |
| EQUISETUM HYEMALE | ACTIVE INGREDIENT | 59677RXH25 | 1 | |
| FERROUS IODIDE | ACTIVE INGREDIENT | F5452U54PN | 1 | |
| FUMARIA OFFICINALIS FLOWERING TOP | ACTIVE INGREDIENT | VH659J61ZL | 1 | |
| GENTIANA LUTEA ROOT | ACTIVE INGREDIENT | S72O3284MS | 1 | |
| GERANIUM ROBERTIANUM | ACTIVE INGREDIENT | R5I1HK0UBL | 1 | |
| JUGLANS REGIA FLOWERING TOP | ACTIVE INGREDIENT | 3BA2N709NG | 1 | |
| MERCURIC CYANIDE | ACTIVE INGREDIENT | RWG7BD1032 | 1 | |
| MYOSOTIS ARVENSIS | ACTIVE INGREDIENT | C73BK97H5J | 1 | |
| PHYTOLACCA AMERICANA ROOT | ACTIVE INGREDIENT | 11E6VI8VEG | 1 | |
| PINUS SYLVESTRIS LEAFY TWIG | ACTIVE INGREDIENT | Q1RGP4UB73 | 1 | |
| RORIPPA NASTURTIUM-AQUATICUM | ACTIVE INGREDIENT | YH89GMV676 | 1 | |
| SARSAPARILLA ROOT | ACTIVE INGREDIENT | M5552F7Y3Q | 1 | |
| SCROPHULARIA NODOSA | ACTIVE INGREDIENT | 7H443NUB2T | 1 | |
| SODIUM SULFATE | ACTIVE INGREDIENT | 0YPR65R21J | 1 | |
| SUS SCROFA PARATHYROID GLAND | ACTIVE INGREDIENT | 2KBE35NE8S | 1 | |
| SUS SCROFA THYMUS | ACTIVE INGREDIENT | 7B69B0BD62 | 1 | |
| SUS SCROFA THYROID | ACTIVE INGREDIENT | 6RV024OAUQ | 1 | |
| TEUCRIUM SCORODONIA FLOWERING TOP | ACTIVE INGREDIENT | LOK3I16O7G | 1 | |
| TRIBASIC CALCIUM PHOSPHATE | ACTIVE INGREDIENT | 91D9GV0Z28 | 1 | |
| VERONICA OFFICINALIS FLOWERING TOP | ACTIVE INGREDIENT | 9IH82J936J | 1 | |
| ALOE | ACTIVE MOIETY | V5VD430YW9 | 1 | |
| APIS MELLIFERA | ACTIVE MOIETY | 7S82P3R43Z | 1 | |
| ARANEUS DIADEMATUS | ACTIVE MOIETY | 6T6CO7R3Z5 | 1 | |
| BARIUM | ACTIVE MOIETY | 24GP945V5T | 1 | |
| CALCIUM | ACTIVE MOIETY | SY7Q814VUP | 1 | |
| CALCIUM CATION | ACTIVE MOIETY | 2M83C4R6ZB | 1 | |
| EQUISETUM HYEMALE | ACTIVE MOIETY | 59677RXH25 | 1 | |
| FERROUS IODIDE | ACTIVE MOIETY | F5452U54PN | 1 | |
| FUMARIA OFFICINALIS FLOWERING TOP | ACTIVE MOIETY | VH659J61ZL | 1 | |
| GENTIANA LUTEA ROOT | ACTIVE MOIETY | S72O3284MS | 1 | |
| GERANIUM ROBERTIANUM | ACTIVE MOIETY | R5I1HK0UBL | 1 | |
| JUGLANS REGIA FLOWERING TOP | ACTIVE MOIETY | 3BA2N709NG | 1 | |
| MERCURIC CATION | ACTIVE MOIETY | ED30FJ8Y42 | 1 | |
| MYOSOTIS ARVENSIS | ACTIVE MOIETY | C73BK97H5J | 1 | |
| PHYTOLACCA AMERICANA ROOT | ACTIVE MOIETY | 11E6VI8VEG | 1 | |
| PINUS SYLVESTRIS LEAFY TWIG | ACTIVE MOIETY | Q1RGP4UB73 | 1 | |
| RORIPPA NASTURTIUM-AQUATICUM | ACTIVE MOIETY | YH89GMV676 | 1 | |
| SARSAPARILLA ROOT | ACTIVE MOIETY | M5552F7Y3Q | 1 | |
| SCROPHULARIA NODOSA | ACTIVE MOIETY | 7H443NUB2T | 1 | |
| SODIUM CATION | ACTIVE MOIETY | LYR4M0NH37 | 1 | |
| SUS SCROFA PARATHYROID GLAND | ACTIVE MOIETY | 2KBE35NE8S | 1 | |
| SUS SCROFA THYMUS | ACTIVE MOIETY | 7B69B0BD62 | 1 | |
| SUS SCROFA THYROID | ACTIVE MOIETY | 6RV024OAUQ | 1 | |
| TEUCRIUM SCORODONIA FLOWERING TOP | ACTIVE MOIETY | LOK3I16O7G | 1 | |
| VERONICA OFFICINALIS FLOWERING TOP | ACTIVE MOIETY | 9IH82J936J | 1 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Products#
Every source-derived product name is available through these pages.
- Lymphdrainex
- Geranium robertianum, Nasturtium aquaticum, Aloe socotrina, Juglans regia, Myosotis arvensis, Scrophularia nodosa, Teucrium scorodonia, Apis mellifica, Equisetum hyemale,
- GERANIUM ROBERTIANUM
- RORIPPA NASTURTIUM-AQUATICUM
- ALOE
- JUGLANS REGIA FLOWERING TOP
- MYOSOTIS ARVENSIS
- SCROPHULARIA NODOSA
- TEUCRIUM SCORODONIA FLOWERING TOP
- APIS MELLIFERA
- EQUISETUM HYEMALE
- FUMARIA OFFICINALIS FLOWERING TOP
- SODIUM SULFATE
- SODIUM SULFATE ANHYDROUS
- PHYTOLACCA AMERICANA ROOT
- PINUS SYLVESTRIS LEAFY TWIG
- VERONICA OFFICINALIS FLOWERING TOP
- GENTIANA LUTEA ROOT
- SARSAPARILLA ROOT
- BARIUM CARBONATE
- BARIUM CATION
- CALCIUM SULFIDE
- MERCURIC CYANIDE
- FERROUS IODIDE
- ARANEUS DIADEMATUS
- TRIBASIC CALCIUM PHOSPHATE
- CALCIUM CATION
- SUS SCROFA PARATHYROID GLAND
- SUS SCROFA THYROID
- WATER
- ALCOHOL
- SUS SCROFA THYMUS
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 57520-0596 | 57520-0596-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
Inactive ingredient matches#
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TOPICAL | 541 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / SUBLINGUAL | 397 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SHAMPOO / TOPICAL | 714 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | ELIXIR / ORAL | 13675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | JELLY / VAGINAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TRANSDERMAL | 7360 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TRANSDERMAL | 3675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / SUBCUTANEOUS | 6.1 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TOPICAL | 2445 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TRANSDERMAL | 90 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | MOUTHWASH / BUCCAL | 200 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAVENOUS | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | POWDER, FOR SOLUTION / TOPICAL | 40 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVESICAL | 7892 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVENOUS | 92 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / ORAL | 198 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SWAB / TOPICAL | 2250 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / RESPIRATORY (INHALATION) | 0.08 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TRANSDERMAL | 49.37 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / NASAL | 70 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / RECTAL | 0.35 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | PASTE / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVASCULAR | 100 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / SUBCUTANEOUS | 149 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / DENTAL | 12.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TOPICAL | 3633 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / RESPIRATORY (INHALATION) | 5 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / OPHTHALMIC | 0.5 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LOTION / TOPICAL | 25 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / ORAL | 681 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAMUSCULAR | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAVENOUS | 6405 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / BUCCAL | 679 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / RESPIRATORY (INHALATION) | 26664 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / RESPIRATORY (INHALATION) | 35.75 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / INTRAVENOUS | 4000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, EMULSION / INTRAVENOUS | 520 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVENOUS | 99 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, FOAM / TOPICAL | 4504 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAMUSCULAR | 1000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / RECTAL | 898 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAMUSCULAR | 1491 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY, METERED / SUBLINGUAL | 29 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / ORAL | 210 mg/1ml |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| d5d98bb1-c802-4dd7-944c-b199dd5b0a10 | b5d2c16d-5950-4ed9-914a-53f5e0240406 | 2022-04-06 | Warnings | d5d98bb1-c802-4dd7-944c-b199dd5b0a10 b5d2c16d-5950-4ed9-914a-53f5e0240406 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
