Allergena
- Manufacturer
- Meditrend, Inc. DBA Progena Professional Formulations
- Effective date
- 2020-06-18
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 23:25:15
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients: Antigens 6x, 12x, 30x:
*Seasonal Grasses, *Seasonal Trees, *Seasonal Weeds: Herbal
Drainage Remedies 3x: Baptisia tinctoria HPUS, Hydrastis
canadensis HPUS, Phytolacca decandra HPUS, Trigonella foenum-
graecum; Echinacea 3X HPUS.
OTC - PURPOSE SECTION
Purpose: Relief from Sneezing, Runny Nose, Itchy Eyes and
Sinus Congestion.
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
Use: This product is a Homeopathic Dilution formulated to support the body's immunity for the temporary relief of allergies.
WARNINGS SECTION
Warnings:
- Use only as directed.
- Stop use and ask a doctor if symptoms worsen or do not improve after 5 days.
- If pregnant or breastfeeding, consult a health professional before use.
DOSAGE & ADMINISTRATION SECTION
Directions: •Adults (12 and Older) Chew and dissolve 1
tablet three times daily. • Children (7-12) Chew and
dissolve 1 tablet three times daily. • Children (2-7) Chew and
dissolve 1 tablet 2-3 times daily. • Not recommended for
children under 2 years old. • Consult a Physician for 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: Croscarmellose Sodium, Magnesium
Stearate, Microcrystalline Cellulose, Xylitol, Zemea.
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 |
|---|---|---|---|---|---|
| 62713-944-01 | 2020-06-18 | C162847 | 48780-1 | 9d75b9d1-05f4-f424-e053-dadaa90a57ce | Allergena Tabs |
| 62713-944-01 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-05f4-f424-e053-dadaa90a57ce | Allergena Tabs |
Products#
Every source-derived product name is available through these pages.
- Allergena Seasonal Allergy Tabs
- Allergy Relief
- CROSCARMELLOSE SODIUM
- MAGNESIUM STEARATE
- CELLULOSE, MICROCRYSTALLINE
- XYLITOL
- PROPANEDIOL
- BAPTISIA TINCTORIA ROOT
- GOLDENSEAL
- MYRRH
- NASTURTIUM OFFICINALE
- PHYTOLACCA AMERICANA ROOT
- FENUGREEK LEAF
- ECHINACEA, UNSPECIFIED
- ACACIA POLLEN
- ALNUS RUBRA POLLEN
- ALNUS INCANA SUBSP. RUGOSA POLLEN
- FRAXINUS VELUTINA POLLEN
- FRAXINUS PENNSYLVANICA POLLEN
- FRAXINUS AMERICANA POLLEN
- POPULUS TREMULOIDES POLLEN
- MORELLA CERIFERA POLLEN
- FAGUS GRANDIFOLIA POLLEN
- BETULA PAPYRIFERA POLLEN
- BETULA NIGRA POLLEN
- BETULA LENTA POLLEN
- ROBINIA PSEUDOACACIA POLLEN
- ACER NEGUNDO POLLEN
- JUNIPERUS ASHEI POLLEN
- JUNIPERUS PINCHOTII POLLEN
- JUNIPERUS VIRGINIANA POLLEN
- POPULUS DELTOIDES SUBSP. DELTOIDES POLLEN
- POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN
- CUPRESSUS ARIZONICA POLLEN
- TAXODIUM DISTICHUM POLLEN
- PHOENIX DACTYLIFERA POLLEN
- ULMUS AMERICANA POLLEN
- ULMUS CRASSIFOLIA POLLEN
- ULMUS PUMILA POLLEN
- ULMUS RUBRA POLLEN
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 62713-944 | 62713-944-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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 |
|---|---|---|---|---|---|---|
| b6c1ac50-2acf-261e-e053-2995a90a0499 | f3da0e57-18a3-49ac-833c-b0b3fb3b49d7 | 2020-12-18 | Warnings | f3da0e57-18a3-49ac-833c-b0b3fb3b49d7 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
