Sootheez Organic Variety Pack Pectin 11.5 mg/3.5g Lozenge
by BFY LLC · 4 CANISTER in 1 CARTON (72427-4756-1) / 56 g in 1 CANISTER
NDC 72427-4756-01
🏷️ FDA NDC (as labeled)
72427-4756-1
billing pads the package segment with a zero
OTC
Discontinued
Non-controlled
⚠ Inactivated by FDA
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
⚠️
Excluded from the active FDA NDC Directory.
FDA inactivated this product’s listing record, so it is excluded from the active NDC Directory. The listing was last certified through Dec 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory.
Search the FDA NDC Directory ↗
🆔 Identity & classification
FDA NDC (as labeled)
72427-4756-1
Product NDC
72427-4756
11-digit billing NDC
72427475601
RxCUI
2204565
UNII
89NA02M4RX
Application #
M022
SPL Set ID
3cf4af1f-a360-6e11-e063-6294a90ab408
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
Discontinued
FDA listing status
Inactivated by FDA (certified through Dec 2026)
Marketing start
2025-08-22
Route
ORAL
Dosage form
LOZENGE
Substance
PECTIN
Why two NDCs?
The FDA registers this code as 72427-4756-1 — 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 → 72427-4756-01. 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.
🏷️ RxNorm drug class
This medicine belongs to the Other intestinal adsorbents class.
Drug family (ATC)
Other intestinal adsorbents
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.
🏭 Manufacturer & labeler
LabelerBFY LLC
FDA applicationM022 (OTC MONOGRAPH DRUG)
Labeler code72427
First marketedAug 2025
Product typeHuman Otc Drug
Portfolio19 products on file
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?
Sootheez Organic Variety Pack is an over-the-counter lozenge containing pectin, a natural fiber derived from fruit. Pectin lozenges are commonly used in throat-soothing products because pectin can coat and help relieve minor throat irritation and discomfort. This product is marketed under the FDA's OTC monograph rules for its category. Lozenges are meant to dissolve slowly in the mouth to deliver the soothing ingredient to the throat area.
Patient education
Supplement & herbal interactions
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.
💬 Questions about Pectin?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
💊 What it looks like
Color
red / yellow
ShapeOval
ImprintP
Size23 mm
ScoringNot scored
FlavorLemon
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 Y9H1V576FH
Honey is a natural sweetener made by bees from flower nectar. In medicines, it adds sweetness to improve taste and may help soothe throat irritation in lozenges or syrups.
1 inactive ingredient listed in the exact product block matched to this NDC.
The official label also statesBerry Lemonade: citric acid, organic cane sugar, organic honey, organic lemon flavor, organic lemon juice concentrate, organic lemon powder, organic raspberry flavor, organic raspberry juice concentrate, organic raspberry powder, organic rice syrup, organic strawberry juice concentrate, organic vegetable juice concentrate (carrot, radish). Birthday Cake: organic cane sugar, organic honey, organic natural flavors, organic rice syrup. Watermelon Mint: citric acid, organic apple juice concentrate, organic cane sugar, organic grape juice concentrate, organic honey, organic mint flavor, organic raspberry powder, organic rice syrup, organic strawberry powder, organic vegetable juice concentrate (carrot, radish), organic watermelon flavor, organic wildberry juice concentrate. Wild Cherry: citric acid, organic cane sugar, organic cherry juice concentrate, organic honey, organic natural flavor, organic rice syrup, organic strawberry juice concentrate, organic strawberry powder, organic tart cherry powder.
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 |
|---|---|---|---|---|---|---|
| Sootheez Berry Lemonade 11.5 mg/3.5g 61584-0017-01 | Primrose | 49 g | — | — | FDA listed | — |
| Sootheez Strawberry Lemonade 11.5 mg/3.5g 61584-0018-01 | Primrose | 49 g | — | — | FDA listed | — |
| Sootheez Birthday Cake 11.5 mg/3.5g 61584-0019-01 | Primrose | 49 g | — | — | FDA listed | — |
| Sootheez Watermelon Mint 11.5 mg/3.5g 61584-0020-01 | Primrose | 49 g | — | — | FDA listed | — |
| Lolleez Variety Pack 11.5 mg/7g 72427-3195-01 | BFY | 105 g | — | — | FDA listed | — |
| Lolleez Watermelon 11.5 mg/7g 72427-3295-01 | BFY | 105 g | — | — | FDA listed | — |
| Lolleez Strawberry 11.5 mg/7g 72427-3395-01 | BFY | 105 g | — | — | FDA listed | — |
| Lolleez Orange Mango 11.5 mg/7g 72427-3495-01 | BFY | 105 g | — | — | FDA listed | — |
| Lolleez Mixed Berry 11.5 mg/7g 72427-3515-01 | BFY | 105 g | — | — | FDA listed | — |
| Lolleez Organic Variety Pack (WM, SB, BC, MB) 11.5 mg/7g 72427-3640-01 | BFY | 280 g | — | — | FDA listed | — |
| Sootheez Organic Wild Cherry 11.5 mg/3.5g 72427-3714-00 | BFY | 13153 g | — | — | FDA listed | — |
| Sootheez Organic Raspberry 11.5 mg/3.5g 72427-3814-00 | BFY | 13153 g | — | — | FDA listed | — |
| Sootheez Berry Lemonade 11.5 mg/3.5g 72427-4014-00 | BFY | 13154 g | — | — | FDA listed | — |
| Sootheez Birthday Cake 11.5 mg/3.5g 72427-4114-00 | BFY | 13154 g | — | — | FDA listed | — |
| Sootheez Strawberry Lemonade 11.5 mg/3.5g 72427-4214-00 | BFY | 13154 g | — | — | FDA listed | — |
| Sootheez Watermelon Mint 11.5 mg/3.5g 72427-4314-00 | BFY | 13154 g | — | — | FDA listed | — |
| Lolleez Variety Pack 11.5 mg/7g 72427-4540-01 | BFY | 280 g | — | — | FDA listed | — |
| Lolleez Birthday Cake - Conventional 11.5 mg/7g 72427-4615-00 | BFY | 7140 g | — | — | FDA listed | — |
| Sootheez Organic Variety Pack 11.5 mg/3.5gthis 72427-4756-01 | BFY | 4 canisters | — | — | Discontinued | — |
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
🏛️
2025
On the market since
Aug 2025
📍
2026
Currently FDA-listed
1 year 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.
🔬 Reported adverse events (FAERS)
Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Pectin — the ingredient across all brands.
Top reported reactions
Age at onset
Reporter sex
Male · 34%
Female · 66%
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 72427-4756-01 You're viewing this | 4 CANISTER in 1 CARTON (72427-4756-1) / 56 g in 1 CANISTER | 2025-08-22 | Inactivated by FDA |
🧭 About this NDC listing & data coverage
Over-the-counter (OTC) product
No longer marketed (per FDA listing data)
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 "Otc Monograph Drug". 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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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 72427-4756-1, 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: 72427-4756-01, written without dashes as 72427475601. 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 72427-4756-01, the first segment (72427) is the labeler code FDA assigned to BFY LLC; the middle segment (4756) 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.
Who lists this product with the FDA?
BFY LLC 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 ▾
Uses for temporary relief of minor discomfort of the throat.
⏱️ Dosage and Administration ▾
Directions Adults and children 10 years of age and older: allow one drop to dissolve slowly in mouth. May be repeated as needed or as directed by a doctor. Children under 10 years of age: ask a doctor.
⚠️ Warnings ▾
Warnings Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomitting, consult a doctor promptly. If sore mouth symptoms do not improve in 7 days, see your dentist or doctor promptly. Stop use and ask a doctor if sore throat does not improve in 7 days. irritation, pain, or redness persists or worsens.
🧪 Active Ingredient ▾
Active Ingredient (in each drop) Pectin 11.5 mg
🧪 Inactive Ingredients ▾
Inactive ingredients Berry Lemonade: citric acid, organic cane sugar, organic honey, organic lemon flavor, organic lemon juice concentrate, organic lemon powder, organic raspberry flavor, organic raspberry juice concentrate, organic raspberry powder, organic rice syrup, organic strawberry juice concentrate, organic vegetable juice concentrate (carrot, radish). Birthday Cake: organic cane sugar, organic honey, organic natural flavors, organic rice syrup. Watermelon Mint: citric acid, organic apple juice concentrate, organic cane sugar, organic grape juice concentrate, organic honey, organic mint flavor, organic raspberry powder, organic rice syrup, organic strawberry powder, organic vegetable juice concentrate (carrot, radish), organic watermelon flavor, organic wildberry juice concentrate.
Wild Cherry: citric acid, organic cane sugar, organic cherry juice concentrate, organic honey, organic natural flavor, organic rice syrup, organic strawberry juice concentrate, organic strawberry powder, organic tart cherry powder.
🎯 Purpose ▾
Purpose Oral Demulcent
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
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.