Allergena
- Manufacturer
- Meditrend, Inc. DBA Progena Professional Formulations
- Effective date
- 2015-11-25
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 02:06:58
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients:Echinacea 3X HPUS; Drainage Remedies:Baptisia Tinctoria 3X HPUS, Hydrastis Canadensis 3X HPUS, Myrrha 3X HPUS, Nasturtium Aquaticum 3X HPUS, Phytolacca Decandra 3X HPUS, Trigonella Foenum-Graecum 3X; Dust Mite and House Dust Antigen 9X, 12X, 15X, 30X:Blatta Orientalis (Oriental Cockroach) HPUS, Dust Mite (D.Pteronyssinus, D. Farinae), Grain Dust (Barley, Corn, Millet, Oat, Rice, Wheat), House Dust (Mattress, Rug, Upholstery), Periplaneta Americana (American Cockroach) HPUS; Stannum Metallicum 12X HPUS.
OTC - PURPOSE SECTION
Purpose:Relief from Sneezing, Runny Nose, Itchy Eyes and Sinus Congestion.
INDICATIONS & USAGE SECTION
Use:This product is a Homeopathic Dilution formulated to support the body's immunity for the temporary relief of allergies.
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:• Shake Well Before Use.• Adults (12 and Older)take 15 drops under the tongue three times daily.• Children (11 and Younger)take 6 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.
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.allergena.com

FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 62713-812-01 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-261d-f424-e053-dadaa90a57ce | Dust + Mite |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62713-812-01 | AllergenaDust Plus Mite | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 62713-812 | ALLERGENA DUST PLUS MITE (ECHINACEA, BAPTISIA TINCTORIA, HYDRASTIS CANADENSIS, MYRRHA, NASTURTIUM AQUATICUM, PHYTOLACCA DECANDRA, TRIGONELLA FOENUM-GRAECUM, BLATTA ORIENTALIS (ORIENTAL COCKROACH) HPUS, DUST MITE (D.PTERONYSSINUS, D. FARINAE), GRAIN DUST (BARLEY, CORN, MILLET, OAT, RICE, WHEAT), HOUSE DUST (MATTRESS, RUG, UPHOLSTERY), PERIPLANETA AMERICANA, STANNUM METALLICUM) LIQUID [MEDITREND, INC. DBA PROGENA PROFESSIONAL FORMULATIONS] | 2 | Legacy NDC, 1 package rows | 20151125_4fe91b6f-237c-4752-a720-76138e6888a9.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| BAPTISIA TINCTORIA ROOT | ACTIVE INGREDIENT | 5EF0HWI5WU | 2 | |
| BARLEY | ACTIVE INGREDIENT | 5PWM7YLI7R | 2 | |
| BLATTA ORIENTALIS | ACTIVE INGREDIENT | 535787266D | 2 | |
| BROWN RICE | ACTIVE INGREDIENT | 659G217HPG | 2 | |
| CORN | ACTIVE INGREDIENT | 0N8672707O | 2 | |
| DERMATOPHAGOIDES FARINAE | ACTIVE INGREDIENT | PR9U2YPF3Q | 2 | |
| DERMATOPHAGOIDES PTERONYSSINUS | ACTIVE INGREDIENT | 57L1Z5378K | 2 | |
| ECHINACEA, UNSPECIFIED | ACTIVE INGREDIENT | 4N9P6CC1DX | 2 | |
| FENUGREEK LEAF | ACTIVE INGREDIENT | 487RI96K8Z | 2 | |
| GOLDENSEAL | ACTIVE INGREDIENT | ZW3Z11D0JV | 2 | |
| HOUSE DUST | ACTIVE INGREDIENT | EYO007VX98 | 2 | |
| MILLET | ACTIVE INGREDIENT | TJR6B3R47P | 2 | |
| MYRRH | ACTIVE INGREDIENT | JC71GJ1F3L | 2 | |
| NASTURTIUM OFFICINALE | ACTIVE INGREDIENT | YH89GMV676 | 2 | |
| OAT | ACTIVE INGREDIENT | Z6J799EAJK | 2 | |
| PERIPLANETA AMERICANA | ACTIVE INGREDIENT | 2RQ1L9N089 | 2 | |
| PHYTOLACCA AMERICANA ROOT | ACTIVE INGREDIENT | 11E6VI8VEG | 2 | |
| TIN | ACTIVE INGREDIENT | 387GMG9FH5 | 2 | |
| WHEAT BRAN | ACTIVE INGREDIENT | 6L966A1IMR | 2 | |
| BAPTISIA TINCTORIA ROOT | ACTIVE MOIETY | 5EF0HWI5WU | 2 | |
| BARLEY | ACTIVE MOIETY | 5PWM7YLI7R | 2 | |
| BLATTA ORIENTALIS | ACTIVE MOIETY | 535787266D | 2 | |
| BROWN RICE | ACTIVE MOIETY | 659G217HPG | 2 | |
| CORN | ACTIVE MOIETY | 0N8672707O | 2 | |
| DERMATOPHAGOIDES FARINAE | ACTIVE MOIETY | PR9U2YPF3Q | 2 | |
| DERMATOPHAGOIDES PTERONYSSINUS | ACTIVE MOIETY | 57L1Z5378K | 2 | |
| ECHINACEA, UNSPECIFIED | ACTIVE MOIETY | 4N9P6CC1DX | 2 | |
| FENUGREEK LEAF | ACTIVE MOIETY | 487RI96K8Z | 2 | |
| GOLDENSEAL | ACTIVE MOIETY | ZW3Z11D0JV | 2 | |
| HOUSE DUST | ACTIVE MOIETY | EYO007VX98 | 2 | |
| MILLET | ACTIVE MOIETY | TJR6B3R47P | 2 | |
| MYRRH | ACTIVE MOIETY | JC71GJ1F3L | 2 | |
| NASTURTIUM OFFICINALE | ACTIVE MOIETY | YH89GMV676 | 2 | |
| OAT | ACTIVE MOIETY | Z6J799EAJK | 2 | |
| PERIPLANETA AMERICANA | ACTIVE MOIETY | 2RQ1L9N089 | 2 | |
| PHYTOLACCA AMERICANA ROOT | ACTIVE MOIETY | 11E6VI8VEG | 2 | |
| TIN | ACTIVE MOIETY | 387GMG9FH5 | 2 | |
| WHEAT BRAN | ACTIVE MOIETY | 6L966A1IMR | 2 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | 2 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 2 |
Products#
Every source-derived product name is available through these pages.
- Allergena Dust Plus Mite
- Echinacea, Baptisia Tinctoria, Hydrastis Canadensis, Myrrha, Nasturtium Aquaticum, Phytolacca Decandra, Trigonella Foenum-Graecum, Blatta Orientalis (Oriental Cockroach) HPUS, Dust Mite (D.Pteronyssinus, D. Farinae), Grain Dust (Barley, Corn, Millet, Oat, Rice, Wheat), House Dust (Mattress, Rug, Upholstery), Periplaneta Americana, Stannum Metallicum
- WATER
- ALCOHOL
- ECHINACEA, UNSPECIFIED
- BAPTISIA TINCTORIA ROOT
- GOLDENSEAL
- MYRRH
- NASTURTIUM OFFICINALE
- PHYTOLACCA AMERICANA ROOT
- FENUGREEK LEAF
- BLATTA ORIENTALIS
- DERMATOPHAGOIDES PTERONYSSINUS
- DERMATOPHAGOIDES FARINAE
- BARLEY
- CORN
- MILLET
- OAT
- BROWN RICE
- WHEAT BRAN
- HOUSE DUST
- PERIPLANETA AMERICANA
- TIN
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 62713-812 | 62713-812-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| ECHINACEA, UNSPECIFIED | 4N9P6CC1DX | ACTIB |
| BAPTISIA TINCTORIA ROOT | 5EF0HWI5WU | ACTIB |
| GOLDENSEAL | ZW3Z11D0JV | ACTIB |
| MYRRH | JC71GJ1F3L | ACTIB |
| NASTURTIUM OFFICINALE | YH89GMV676 | ACTIB |
| PHYTOLACCA AMERICANA ROOT | 11E6VI8VEG | ACTIB |
| FENUGREEK LEAF | 487RI96K8Z | ACTIB |
| BLATTA ORIENTALIS | 535787266D | ACTIB |
| DERMATOPHAGOIDES PTERONYSSINUS | 57L1Z5378K | ACTIB |
| DERMATOPHAGOIDES FARINAE | PR9U2YPF3Q | ACTIB |
| BARLEY | 5PWM7YLI7R | ACTIB |
| CORN | 0N8672707O | ACTIB |
| MILLET | TJR6B3R47P | ACTIB |
| OAT | Z6J799EAJK | ACTIB |
| BROWN RICE | 659G217HPG | ACTIB |
| WHEAT BRAN | 6L966A1IMR | ACTIB |
| HOUSE DUST | EYO007VX98 | ACTIB |
| PERIPLANETA AMERICANA | 2RQ1L9N089 | ACTIB |
| TIN | 387GMG9FH5 | 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 | DROPS / ORAL | 210 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SWAB / TOPICAL | 2250 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / BUCCAL | 679 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / RESPIRATORY (INHALATION) | 5 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, FOAM / TOPICAL | 4504 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAVENOUS | 6405 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TOPICAL | 3633 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LOTION / TOPICAL | 25 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TOPICAL | 541 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TOPICAL | 2445 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / SUBLINGUAL | 397 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / RESPIRATORY (INHALATION) | 0.08 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / NASAL | 70 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVENOUS | 99 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | MOUTHWASH / BUCCAL | 200 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SHAMPOO / TOPICAL | 714 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / DENTAL | 12.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | ELIXIR / ORAL | 13675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAMUSCULAR | 1491 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVESICAL | 7892 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAVENOUS | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVENOUS | 92 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / INTRAVENOUS | 4000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / ORAL | 681 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TRANSDERMAL | 49.37 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / ORAL | 198 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / RESPIRATORY (INHALATION) | 35.75 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAMUSCULAR | 1000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / RESPIRATORY (INHALATION) | 26664 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, EMULSION / INTRAVENOUS | 520 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / SUBCUTANEOUS | 6.1 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TRANSDERMAL | 90 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / RECTAL | 0.35 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | PASTE / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TRANSDERMAL | 7360 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAMUSCULAR | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY, METERED / SUBLINGUAL | 29 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | POWDER, FOR SOLUTION / TOPICAL | 40 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / OPHTHALMIC | 0.5 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / RECTAL | 898 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TRANSDERMAL | 3675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVASCULAR | 100 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | JELLY / VAGINAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / SUBCUTANEOUS | 149 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / NASAL | 10 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 |
|---|---|---|---|---|---|---|
| 256297fa-c58c-72f6-e054-00144ff88e88 | 4fe91b6f-237c-4752-a720-76138e6888a9 | 2015-11-25 | Warnings | 256297fa-c58c-72f6-e054-00144ff88e88 4fe91b6f-237c-4752-a720-76138e6888a9 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.