Home › NDC Lookup › Ingredients › Alternaria Alternata, Bermuda Grass Poll... › 72617-0001-01
Allergy Mix Las Vegas Alternaria Alternata, Bermuda Grass Pollen (Cynodon Dactylon), Cladosporium Herbarum, Histaminum Hydrochloricum, Juniperus Communis, Oleander, Olive Pollen (Olea Europaea), Ragweed Pollen (Ambrosia Artemisiaefolia), Sabina, Ustilago Maidis, White Mulberry 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 6 [hp_X]/mL; 6 [hp_X]/mL; 12 [hp_X]/mL Liquid, 30 mL — NDC 72617-0001-01 package photo

Allergy Mix Las Vegas Alternaria Alternata, Bermuda Grass Pollen (Cynodon Dactylon), Cladosporium Herbarum, Histaminum Hydrochloricum, Juniperus Communis, Oleander, Olive Pollen (Olea Europaea), Ragweed Pollen (Ambrosia Artemisiaefolia), Sabina, Ustilago Maidis, White Mulberry 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 6 [hp_X]/mL; 6 [hp_X]/mL; 12 [hp_X]/mL Liquid, 30 mL

by American Standard Nutraceuticals · 30 mL in 1 BOTTLE, DROPPER (72617-0001-1)
NDC 72617-0001-01
🏷️ FDA NDC (as labeled) 72617-0001-1 billing pads the package segment with a zero
OTC On market Non-controlled
🗂️ Data synced Sep 17, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

🆔 Identity & classification

FDA NDC (as labeled) 72617-0001-1
Product NDC 72617-0001
11-digit billing NDC 72617000101
UNII 52B29REC7H, 175F461W10, O64JF11198, 3POA0Q644U, O84B5194RL, 7KV510R6H6 +5 more
UPC 0181163000233
SPL Set ID 50c82203-6b13-4b33-a34f-20e1aeea78c6
Established class (EPC) Non-Standardized Fungal Allergenic Extract; Standardized Pollen Allergenic Extract; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Non-Standardized Pollen Allergenic Extract
Physiologic effect Increased Histamine Release; Cell-mediated Immunity; Increased IgG Production
Chemical class Fungal Proteins; Allergens; Pollen; Dietary Proteins; Plant Proteins; Food Additives
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-03-26
Route ORAL
Dosage form LIQUID
Substance ALTERNARIA ALTERNATA; CYNODON DACTYLON POLLEN; CLADOSPORIUM HERBARUM; HISTAMINE DIHYDROCHLORIDE; JUNIPER BERRY; NERIUM OLEANDER LEAF; OLEA EUROPAEA POLLEN; AMBROSIA ARTEMISIIFOLIA POLLEN; JUNIPERUS SABINA LEAFY TWIG; USTILAGO MAYDIS; MORUS ALBA POLLEN
Why two NDCs? The FDA registers this code as 72617-0001-1 — a 5-4-1 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the package segment → 72617-0001-01. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

🏭 Manufacturer & labeler

LabelerAmerican Standard Nutraceuticals
Labeler code72617
First marketedMar 2026
Product typeHuman Otc Drug
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

🩺 Clinical

🧪 What is this product?

This is an unapproved homeopathic liquid taken by mouth that contains various plant pollens, fungal extracts, and histamine dihydrochloride. In homeopathic practice, these ingredients are traditionally used to address allergy-related concerns, particularly seasonal allergies linked to local Las Vegas environmental allergens such as ragweed, bermuda grass, and juniper pollen. Homeopathic products are marketed based on homeopathic tradition and principles rather than clinical evidence, and the FDA does not evaluate them for effectiveness or safety the way it does standard drugs.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

💲 Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer mLPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Allergy Mix Las Vegas 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 6 [hp_X]/mL; 6 [hp_X]/mL; 12 [hp_X]/mLthis 72617-0001-01 American 30 ml — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

⏳ Availability & generic status

🏛️
2026
On the market since
Mar 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
72617-0001-01 You're viewing this 30 mL in 1 BOTTLE, DROPPER (72617-0001-1) 2026-03-26 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

Allergy Mix Las Vegas Alternaria Alternata, Bermuda Grass Pollen (Cynodon Dactylon), Cladosporium Herbarum, Histaminum Hydrochloricum, Juniperus Communis, Oleander, Olive Pollen (Olea Europaea), Ragweed Pollen (Ambrosia Artemisiaefolia), Sabina, Ustilago Maidis, White Mulberry 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 6 [hp_X]/mL; 6 [hp_X]/mL; 12 [hp_X]/mL LIQUID is listed under the homeopathic marketing category. An NDC listing in this category does not by itself establish FDA approval, and FDA does not evaluate homeopathic products for effectiveness. This page reports the listing data as published.

What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is available.
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Unapproved Homeopathic". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 72617-0001-1, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 72617-0001-01, written without dashes as 72617000101. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 72617-0001-01, the first segment (72617) is the labeler code FDA assigned to American Standard Nutraceuticals; the middle segment (0001) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by American Standard Nutraceuticals. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
American Standard Nutraceuticals is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.

📄 FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 35 words ▾

USES: For temporary relief of allergy symptoms including • sneezing, • runny nose, • itchy, watery eyes, • congestion, and • stuffy nose.† †Claims based on traditional practice, not accepted medical evidence. Not FDA evaluated.

⏱️ Dosage and Administration 60 words ▾

DIRECTIONS: • Adults & children 12 years of age and older: 10 to 15 drops under the tongue, up to 6 times daily or as directed by a health care professional. • Children under age 12: 5 to 6 drops under the tongue, up to 6 times daily. • Avoid food and fluids 15 minutes before or after each use.

⚠️ Warnings 85 words ▾

WARNINGS: If pregnant or breast-feeding, ask a health professional before use. In case of overdose, get medical help or contact a Poison Control Center right away. Stop use and ask a doctor if symptoms persist or worsen after 5 days.

KEEP OUT OF REACH OF CHILDREN • Consult a physician for use in children under 12 years of age. Do not use if tamper evident seal is broken or missing. • Store at 32-110F. • Store away from electronic devices and out of direct sunlight.

🧪 Active Ingredient 36 words ▾

ACTIVE INGREDIENTS: (in each drop) Alternaria Tenuis 12X, Ambrosia Artemisiaefolia 12X, Cladosporium Herbarum 12X, Cynodon Dactylon 12X, Histaminum Hydrochloricum 12X, Juniperus Communis 6X, Morus Alba 12X, Olea Europaea 12X, Oleander 6X, Sabina 6X, Ustilago Maidis 6X.

🧪 Inactive Ingredients 8 words ▾

INACTIVE INGREDIENTS: Alcohol USP 20%, Purified Water USP.

🎯 Purpose 69 words ▾

PURPOSE: Alternaria Tenuis – Allergen (Mold),† Ambrosia Artemisiaefolia – Allergen (Ragweed),† Cladosporium Herbarum – Allergen (Mold),† Cynodon Dactylon – Allergen (Bermudagrass),† Histaminum Hydrochloricum – Allergic Hypersensitivity,† Juniperus Communis – Allergen (Common Juniper),† Morus Alba – Allergen (Mulberry),† Olea Europaea – Allergen (Olive Tree),† Oleander – Allergen (Oleander),† Sabina – Allergen (Savin Juniper),† Ustilago Maidis – Allergen (Mold)† †Claims based on traditional practice, not accepted medical evidence.

Not FDA evaluated.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 72614-0265-02 · Cannanumb 72618-3000-02 · Pfizer →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.