Progena
- Manufacturer
- Meditrend, Inc. DBA Progena Professional Formulations
- Effective date
- 2020-01-30
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 23:42:21
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients:Acidum Phosphoricum 4X, Berberis Vulgaris 2X, Bilberry 2X, Cheidonium Majus 4X, Creosotum 6X, Kidney 6X, Natrum sulpuricum 6X, Pancreas 6X, Syzygium Jambolanum 10X.
OTC - PURPOSE SECTION
Purpose:Support for the Body's Endocrine and Organ System.
INDICATIONS & USAGE SECTION
Use:This product is a Homeopathic Dilution, formulated to support the Body's Endocrine and Organ System.
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 (13 and Older)take 15 drops under the tongue three times daily.• Children (12 and Younger)take 10 drops under the tongue three times daily or as directed by your health care professional.• Consult a Physicianfor use in children under 12 years of age.• Not Recommendedfor children under 2 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:USP Purified 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

FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 62713-914-01 | 2025-02-01 | C162847 | 48780-1 | 2cef2736-a7ce-d83d-e063-dadaa90ab31f | Pancreas Plus |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| BERBERIS VULGARIS ROOT BARK | ACTIVE INGREDIENT | 1TH8Q20J0U | 2 | |
| BILBERRY | ACTIVE INGREDIENT | 9P2U39H18W | 2 | |
| CHELIDONIUM MAJUS | ACTIVE INGREDIENT | 7E889U5RNN | 2 | |
| PHOSPHORIC ACID | ACTIVE INGREDIENT | E4GA8884NN | 2 | |
| PORK KIDNEY | ACTIVE INGREDIENT | X7BCI5P86H | 2 | |
| SODIUM SULFATE | ACTIVE INGREDIENT | 0YPR65R21J | 2 | |
| SUS SCROFA PANCREAS | ACTIVE INGREDIENT | 9Y3J3362RY | 2 | |
| SYZYGIUM CUMINI SEED | ACTIVE INGREDIENT | 820LSF646I | 2 | |
| WOOD CREOSOTE | ACTIVE INGREDIENT | 3JYG22FD73 | 2 | |
| BERBERIS VULGARIS ROOT BARK | ACTIVE MOIETY | 1TH8Q20J0U | 2 | |
| BILBERRY | ACTIVE MOIETY | 9P2U39H18W | 2 | |
| CHELIDONIUM MAJUS | ACTIVE MOIETY | 7E889U5RNN | 2 | |
| PHOSPHORIC ACID | ACTIVE MOIETY | E4GA8884NN | 2 | |
| PORK KIDNEY | ACTIVE MOIETY | X7BCI5P86H | 2 | |
| SODIUM SULFATE ANHYDROUS | ACTIVE MOIETY | 36KCS0R750 | 2 | |
| SUS SCROFA PANCREAS | ACTIVE MOIETY | 9Y3J3362RY | 2 | |
| SYZYGIUM CUMINI SEED | ACTIVE MOIETY | 820LSF646I | 2 | |
| WOOD CREOSOTE | ACTIVE MOIETY | 3JYG22FD73 | 2 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | 2 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 2 |
Products#
Every source-derived product name is available through these pages.
- Progena Pancreas Plus
- Acidum Phosphoricum, Berberis Vulgaris, Bilberry, Cheidonium Majus, Creosotum, Kidney, Natrum sulpuricum, Pancreas, Syzygium Jambolanum
- WATER
- ALCOHOL
- PHOSPHORIC ACID
- BERBERIS VULGARIS ROOT BARK
- BILBERRY
- CHELIDONIUM MAJUS
- WOOD CREOSOTE
- PORK KIDNEY
- SODIUM SULFATE
- SODIUM SULFATE ANHYDROUS
- SUS SCROFA PANCREAS
- SYZYGIUM CUMINI SEED
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 62713-914 | 62713-914-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| PHOSPHORIC ACID | E4GA8884NN | ACTIB |
| BERBERIS VULGARIS ROOT BARK | 1TH8Q20J0U | ACTIB |
| BILBERRY | 9P2U39H18W | ACTIB |
| CHELIDONIUM MAJUS | 7E889U5RNN | ACTIB |
| WOOD CREOSOTE | 3JYG22FD73 | ACTIB |
| PORK KIDNEY | X7BCI5P86H | ACTIB |
| SODIUM SULFATE | 0YPR65R21J | ACTIB |
| SUS SCROFA PANCREAS | 9Y3J3362RY | ACTIB |
| SYZYGIUM CUMINI SEED | 820LSF646I | 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 | LOTION / TOPICAL | 25 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / DENTAL | 12.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / ORAL | 198 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / RESPIRATORY (INHALATION) | 35.75 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVESICAL | 7892 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TOPICAL | 3633 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TRANSDERMAL | 90 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | ELIXIR / ORAL | 13675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / BUCCAL | 679 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SWAB / TOPICAL | 2250 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / NASAL | 70 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TRANSDERMAL | 7360 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / RESPIRATORY (INHALATION) | 26664 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | MOUTHWASH / BUCCAL | 200 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / ORAL | 681 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAMUSCULAR | 1000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAVENOUS | 6405 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / ORAL | 210 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVASCULAR | 100 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / SUBLINGUAL | 397 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / RESPIRATORY (INHALATION) | 0.08 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAMUSCULAR | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TRANSDERMAL | 49.37 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVENOUS | 92 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | PASTE / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, FOAM / TOPICAL | 4504 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | POWDER, FOR SOLUTION / TOPICAL | 40 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / RESPIRATORY (INHALATION) | 5 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / RECTAL | 898 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / SUBCUTANEOUS | 149 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TOPICAL | 541 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / INTRAVENOUS | 4000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / RECTAL | 0.35 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, EMULSION / INTRAVENOUS | 520 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | JELLY / VAGINAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TRANSDERMAL | 3675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / OPHTHALMIC | 0.5 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SHAMPOO / TOPICAL | 714 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVENOUS | 99 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / SUBCUTANEOUS | 6.1 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY, METERED / SUBLINGUAL | 29 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAVENOUS | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TOPICAL | 2445 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAMUSCULAR | 1491 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 |
|---|---|---|---|---|---|---|
| 2cf5f2b8-28e4-ad77-e063-6394a90afc3e | b3430bfb-0d8c-4ea6-9d6f-e2fdf7dd74c1 | 2025-01-30 | Warnings | b3430bfb-0d8c-4ea6-9d6f-e2fdf7dd74c1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.