Progena
- Manufacturer
- Meditrend, Inc. DBA Progena Professional Formulations
- Effective date
- 2015-12-01
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 5
- Source
- full-release
- Hydrated at
- 2026-06-01 02:06:59
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients:Phellandrium aquaticum 3X, Rumex crispus 3X, Sambucus nigra 3X, Senega officinalis 3X, Lung 6X, Arsenicum album 30C, Carbo vegetabilis 30C, Drosera rotundifolia 30C, Ipecacuanha 30C, Phosphorus 30C, Pulsatilla 30C, Silicea 30C, Sulphur 30C.
OTC - PURPOSE SECTION
Purpose:Promotes Healthy Lung Function.
INDICATIONS & USAGE SECTION
Use:This product is a Homeopathic Dilution.
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.
WARNINGS SECTION
Warnings:
- Use Only as directed.
- Stop use and ask a doctor ifsymptoms worsen or do not improve after 5 days.
- If pregnant or breast-feeding, consult a health professional before use.
DOSAGE & ADMINISTRATION SECTION
Directions:• Adults (12 and Older)15 drops under the tongue three times daily.• Children (2-12 years)10 drops under the tongue three times daily or as directed by your health care professional.• Not Recommended for Children Under 2 years of Age.• Consult a Physicianfor use in children under 12 years of age.
OTHER SAFETY INFORMATION
Other Information: Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.
INACTIVE INGREDIENT SECTION
Inactive Ingredients:Demineralized Water and 25% USP Ethanol.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Manufactured for Progena Professional Formulations
4820 Eubank Blvd. NE, ABQ, NM 87111,
www.progena.com

DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 63f39a63-5cd1-4016-bd86-2bbb0f6c3139 | Product name | 3 | 20240506 |
| e5a77e9c-c528-733a-173d-914a234c024b | Product name | 5 | 20240506 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 62713-911-01 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-d699-f424-e053-dadaa90a57ce | Lung Plus |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62713-911-01 | ProgenaLung Plus | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 62713-911 | PROGENA LUNG PLUS (PHELLANDRIUM AQUATICUM, RUMEX CRISPUS, SAMBUCUS NIGRA, SENEGA OFFICINALIS, LUNG, ARSENICUM ALBUM, CARBO VEGETABILIS, DROSERA ROTUNDIFOLIA, IPECACUANHA, PHOSPHORUS, PULSATILLA, SILICEA, SULPHUR) LIQUID [MEDITREND, INC. DBA PROGENA PROFESSIONAL FORMULATIONS] | 5 | Legacy NDC, 1 package rows | 20151201_6ac9326a-bf75-41dd-bd09-0452283f1e64.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| ACTIVATED CHARCOAL | ACTIVE INGREDIENT | 2P3VWU3H10 | 4 | |
| ARSENIC TRIOXIDE | ACTIVE INGREDIENT | S7V92P67HO | 4 | |
| DROSERA ROTUNDIFOLIA | ACTIVE INGREDIENT | QR44N9XPJQ | 4 | |
| IPECAC | ACTIVE INGREDIENT | 62I3C8233L | 4 | |
| OENANTHE AQUATICA FRUIT | ACTIVE INGREDIENT | N4LEE4Z93J | 4 | |
| PHOSPHORUS | ACTIVE INGREDIENT | 27YLU75U4W | 4 | |
| POLYGALA SENEGA ROOT | ACTIVE INGREDIENT | M7T6H7D4IF | 4 | |
| PULSATILLA VULGARIS | ACTIVE INGREDIENT | I76KB35JEV | 4 | |
| RUMEX CRISPUS ROOT | ACTIVE INGREDIENT | 9N1RM2S62C | 4 | |
| SAMBUCUS NIGRA FLOWERING TOP | ACTIVE INGREDIENT | CT03BSA18U | 4 | |
| SILICON DIOXIDE | ACTIVE INGREDIENT | ETJ7Z6XBU4 | 4 | |
| SULFUR | ACTIVE INGREDIENT | 70FD1KFU70 | 4 | |
| SUS SCROFA LUNG | ACTIVE INGREDIENT | 7GL3G1COB3 | 4 | |
| ACTIVATED CHARCOAL | ACTIVE MOIETY | 2P3VWU3H10 | 4 | |
| ARSENIC CATION (3+) | ACTIVE MOIETY | C96613F5AV | 4 | |
| DROSERA ROTUNDIFOLIA | ACTIVE MOIETY | QR44N9XPJQ | 4 | |
| IPECAC | ACTIVE MOIETY | 62I3C8233L | 4 | |
| OENANTHE AQUATICA FRUIT | ACTIVE MOIETY | N4LEE4Z93J | 4 | |
| PHOSPHORUS | ACTIVE MOIETY | 27YLU75U4W | 4 | |
| POLYGALA SENEGA ROOT | ACTIVE MOIETY | M7T6H7D4IF | 4 | |
| PULSATILLA VULGARIS | ACTIVE MOIETY | I76KB35JEV | 4 | |
| RUMEX CRISPUS ROOT | ACTIVE MOIETY | 9N1RM2S62C | 4 | |
| SAMBUCUS NIGRA FLOWERING TOP | ACTIVE MOIETY | CT03BSA18U | 4 | |
| SILICON DIOXIDE | ACTIVE MOIETY | ETJ7Z6XBU4 | 4 | |
| SULFUR | ACTIVE MOIETY | 70FD1KFU70 | 4 | |
| SUS SCROFA LUNG | ACTIVE MOIETY | 7GL3G1COB3 | 4 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | 4 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 4 |
Products#
Every source-derived product name is available through these pages.
- Progena Lung Plus
- Phellandrium aquaticum, Rumex crispus, Sambucus nigra, Senega officinalis, Lung, Arsenicum album, Carbo vegetabilis, Drosera rotundifolia, Ipecacuanha, Phosphorus, Pulsatilla, Silicea, Sulphur
- WATER
- ALCOHOL
- OENANTHE AQUATICA FRUIT
- RUMEX CRISPUS ROOT
- SAMBUCUS NIGRA FLOWERING TOP
- POLYGALA SENEGA ROOT
- SUS SCROFA LUNG
- ARSENIC TRIOXIDE
- ARSENIC CATION (3+)
- ACTIVATED CHARCOAL
- DROSERA ROTUNDIFOLIA
- IPECAC
- PHOSPHORUS
- PULSATILLA VULGARIS
- SILICON DIOXIDE
- SULFUR
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 62713-911 | 62713-911-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| OENANTHE AQUATICA FRUIT | N4LEE4Z93J | ACTIB |
| RUMEX CRISPUS ROOT | 9N1RM2S62C | ACTIB |
| SAMBUCUS NIGRA FLOWERING TOP | CT03BSA18U | ACTIB |
| POLYGALA SENEGA ROOT | M7T6H7D4IF | ACTIB |
| SUS SCROFA LUNG | 7GL3G1COB3 | ACTIB |
| ARSENIC TRIOXIDE | S7V92P67HO | ACTIB |
| ACTIVATED CHARCOAL | 2P3VWU3H10 | ACTIB |
| DROSERA ROTUNDIFOLIA | QR44N9XPJQ | ACTIB |
| IPECAC | 62I3C8233L | ACTIB |
| PHOSPHORUS | 27YLU75U4W | ACTIB |
| PULSATILLA VULGARIS | I76KB35JEV | ACTIB |
| SILICON DIOXIDE | ETJ7Z6XBU4 | ACTIB |
| SULFUR | 70FD1KFU70 | ACTIB |
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 / RECTAL | 898 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / BUCCAL | 679 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LOTION / TOPICAL | 25 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAVENOUS | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / INTRAVENOUS | 4000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAMUSCULAR | 1000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SWAB / TOPICAL | 2250 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY, METERED / SUBLINGUAL | 29 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TRANSDERMAL | 49.37 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / RESPIRATORY (INHALATION) | 0.08 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | POWDER, FOR SOLUTION / TOPICAL | 40 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TOPICAL | 3633 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / OPHTHALMIC | 0.5 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, FOAM / TOPICAL | 4504 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAMUSCULAR | 1491 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / SUBCUTANEOUS | 149 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | JELLY / VAGINAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | PASTE / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVASCULAR | 100 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / ORAL | 210 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TOPICAL | 541 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / ORAL | 681 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | MOUTHWASH / BUCCAL | 200 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / RECTAL | 0.35 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAVENOUS | 6405 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / RESPIRATORY (INHALATION) | 26664 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / NASAL | 70 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / RESPIRATORY (INHALATION) | 5 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TRANSDERMAL | 7360 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TRANSDERMAL | 3675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TRANSDERMAL | 90 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SHAMPOO / TOPICAL | 714 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / ORAL | 198 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | ELIXIR / ORAL | 13675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / SUBLINGUAL | 397 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TOPICAL | 2445 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / RESPIRATORY (INHALATION) | 35.75 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAMUSCULAR | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVENOUS | 92 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, EMULSION / INTRAVENOUS | 520 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / SUBCUTANEOUS | 6.1 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / DENTAL | 12.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVENOUS | 99 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVESICAL | 7892 mg |
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 |
|---|---|---|---|---|---|---|
| 25da8d80-a971-1175-e054-00144ff8d46c | 6ac9326a-bf75-41dd-bd09-0452283f1e64 | 2015-12-01 | Warnings | 25da8d80-a971-1175-e054-00144ff8d46c 6ac9326a-bf75-41dd-bd09-0452283f1e64 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.