NDC 61152-0100-60 — SnoreStop Chewable Fast tabs 60 atropa

🆔 Identity & classification

FDA NDC (as labeled) 61152-100-60

Product NDC 61152-100

11-digit billing NDC 61152010060

UNII WQZ3G9PF0H, R55VQ87DP3, 3POA0Q644U, ZW3Z11D0JV, T4423S18FM, 269XH13919 +1 more

SPL Set ID eb056b9a-e93b-37f7-e053-2995a90a1be1

Established class (EPC) Non-Standardized Plant Allergenic Extract

Physiologic effect Increased Histamine Release; Cell-mediated Immunity; Increased IgG Production

Chemical class Allergens; Plant Proteins; Seed Storage Proteins

DEA schedule Non-controlled

Marketing category UNAPPROVED HOMEOPATHIC

Marketing status On market

FDA listing status Listed (active directory)

Marketing start 2012-08-01

Route ORAL

Dosage form TABLET, CHEWABLE

Substance ATROPA BELLADONNA; EPHEDRA DISTACHYA FLOWERING TWIG; HISTAMINE DIHYDROCHLORIDE; GOLDENSEAL; POTASSIUM DICHROMATE; STRYCHNOS NUX-VOMICA SEED; TEUCRIUM MARUM

Why two NDCs? The FDA registers this code as 61152-100-60 — a 5-3-2 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 product segment → 61152-0100-60. 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

LabelerGreen Pharmaceuticals Inc

Labeler code61152

First marketedAug 2012

Product typeHuman Otc Drug

Portfolio5 products on file

🔎 All NDCs from Green Pharmaceuticals Inc

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?

SnoreStop Chewable Fast tabs is a homeopathic product taken by mouth as a chewable tablet. It contains seven plant-derived and mineral substances traditionally used in homeopathic practice, including atropa belladonna, ephedra, goldenseal, and nux vomica seed, among others. Homeopathic products are marketed based on traditional homeopathic theory rather than clinical evidence, and this product has not been evaluated by the FDA for safety or effectiveness.

Patient education

📘 MedlinePlus patient leaflet ↗

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.

💊 What it looks like

Color white

ShapeRound

ImprintSS

Size1 mm

ScoringNot scored

One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.

Where does this data come from?

Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

🧪 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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

UNII 3SY5LH9PMK
Anhydrous lactose is a milk sugar with no water content. It acts as a filler and binder in tablets and capsules, adding bulk and helping ingredients stick together.
UNII OP1R32D61U
Microcrystalline cellulose is a purified form of cellulose, a natural fiber from plant sources. It acts as a binder and filler in tablets and capsules, helping hold ingredients together and give the medicine its shape and size.
UNII M28OL1HH48
Croscarmellose sodium is a plant-based substance derived from cellulose. It acts as a disintegrant, helping tablets and capsules break down quickly in the digestive system so the medicine can be absorbed.
UNII IY9XDZ35W2
Dextrose is a simple sugar derived from corn or other sources. It serves as a filler and sweetener in medicines to add bulk, improve taste, and help stabilize the medication's form.
UNII J2B2A4N98G
Lactose is a natural sugar derived from milk. In medications, it serves as a filler and binder to add bulk and help hold tablet or capsule ingredients together during manufacturing.
UNII 70097M6I30
Magnesium stearate is a salt made from magnesium and stearic acid, a fatty substance. It's used in tablets and capsules as a lubricant and glidant to help ingredients flow smoothly during manufacturing and prevent sticking.

6 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesAnhydrous Lactose, Croscarmellose sodium, Dextrose (45mg/tab), Lactose (180mg/tab), Magnesium Stearate, Microcrystalline Cellulose.

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?

Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

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 system	Per each	Per 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

Product	Labeler	Pack	NADAC/unit	TE	Status	Price vs. this
SnoreStop Chewable Fast tabs 60 6 [hp_X]/301; 6 [hp_X]/301; 12 [hp_X]/301; 6 [hp_X]/301; 6 [hp_X]/301; 6 [hp_X]/301; 6 [hp_X]/301this 61152-0100-60	Green	60 tablets	—	—	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

🏛️

2012

On the market since

Aug 2012

📍

2026

Currently FDA-listed

14 years listed

🔒

·

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 NDC	Description	Marketing start	Status
61152-0100-60 You're viewing this	60 TABLET, CHEWABLE in 1 PACKAGE (61152-100-60)	2018-08-01	Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

SnoreStop Chewable Fast tabs 60 atropa belladonna,ephedra distachya flowering twig,histamine dihydrochloride,goldenseal,potassium dichromate,strychnos nux-vomica seed,teucrium marum 6 [hp_X]/301; 6 [hp_X]/301; 12 [hp_X]/301; 6 [hp_X]/301; 6 [hp_X]/301; 6 [hp_X]/301; 6 [hp_X]/301 TABLET, CHEWABLE 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)	✓ 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 61152-100-60, 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: 61152-0100-60, written without dashes as 61152010060. 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 61152-0100-60, the first segment (61152) is the labeler code FDA assigned to Green Pharmaceuticals Inc; the middle segment (0100) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (60) 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 Green Pharmaceuticals Inc. Listing status can change — the directory data on this page refreshes weekly.

Who lists this product with the FDA?

Green Pharmaceuticals Inc 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 📋 Description

🎯 Indications and Usage 62 words ▾

Indications & Usage: Adults: Chew one tablet 30 mins before bedtime and repeat at bedtime. Do not take with water. Use 30 mins apart from any food, water, or medicine. Please allow 3-5 days for initial treatment. For Maximum Results, use in conjunction with the SnoreStop Nasal Spray. If symptoms improve after 14 days you may reduce to one tablet at bedtime.

⏱️ Dosage and Administration 68 words ▾

Directions: Children over 5 years of age and Adults Adults: Chew one tablet 30 mins before bedtime and repeat at bedtime. Do not take with water. Use 30 mins apart from any food, water, or medicine. Please allow 3-5 days for initial treatment. For Maximum Results, use in conjunction with the SnoreStop Nasal Spray. If symptoms improve after 14 days you may reduce to one tablet at bedtime.

⚠️ Warnings 51 words ▾

Warnings: Use only as directed. Keep out of reach of children. Do not use on children under 5 years of age. If pregnant or breastfeeding, ask a doctor before use. This product does not treat sleep apnea. Stop use and ask a doctor if symptoms do not improve in 7 days.

🧪 Active Ingredient 77 words ▾

Ingredients (HPUS): Belladonna 6X, Ephedra vulg. 6X, Histaminum hydrochlorinum 12X, Hydrastatis 6X, Kali bic. 6X, Nux vom. 4X, 6X, Teucrium mar. 6X. Active Ingredients

Active Ingredients and purpose Nux vom,4X,6X HPUS……………………………. helps open constricted pharynx Belladonna 6X HPUS………………………………. helps decongest enlarged tonsils Ephedra vulg. 6X HPUS……………………………helps relieve congestion Hydrastis 6X, HPUS…………………………………helps decongest swollen tongue Kali bic. 6X HPUS……………………………………. helps relieve stuffy nose Teucrium mar. 6X HPUS…………………………. helps open air passages Histaminium hydrochlor. 12X HPUS…………helps regulate histamine level

🧪 Inactive Ingredients 14 words ▾

Inactive Ingredients: Anhydrous Lactose, Croscarmellose sodium, Dextrose (45mg/tab), Lactose (180mg/tab), Magnesium Stearate, Microcrystalline Cellulose.

🎯 Purpose 11 words ▾

Uses: Temporarily relieves symptoms of non-apneic snoring. Individual results may vary.

📋 Description 19 words ▾

Description of Product SnoreStop Chewable Tablets A Natural Anti-Snoring Solution NDC 61152-0100-60 60 1 MONTH SUPPLY SnoreStop Chewable Tablets

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

🔗 Related NDC lookups

🧪 All Atropa Belladonna,Ephedra Distachya Flowering Twig,Histamine Dihydrochloride,Goldenseal,Potassium Dichromate,Strychnos Nux-Vomica Seed,Teucrium Marum NDCsSame ingredient 🏭 All Green labeler NDCsLabeler code 61152 📚 All Non-Standardized Plant Allergenic Extract NDCsDrug class