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Lemon Glycerine Swabsticks 7.5 g/100g Swab — NDC 60913-0061-03 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Lemon Glycerine Swabsticks 7.5 g/100g Swab — NDC 60913-061-03 (Billing 60913-0061-03)

by PHOENIX HEALTHCARE SOLUTIONS, LLC · 25 POUCH in 1 BOX / 3 PACKET in 1 POUCH / 1.4 g in 1 PACKET

This is a package of Lemon Glycerine Swabsticks 7.5 g/100g Swab from PHOENIX HEALTHCARE SOLUTIONS, LLC, marketed since Jul 2015 and currently FDA-listed.

NDC 60913-0061-03
🏷️ FDA NDC (as labeled) 60913-061-03 billing pads the product segment with a zero
This package
Contains1.4 g in 1 packet Pack sizes2 compare ↓
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 60913-061-03
Product NDC 60913-061
11-digit billing NDC 60913006103
RxCUI 1114098
UNII PDC6A3C0OX
Application # M003
SPL Set ID 436919f7-14cd-4318-9388-b3e1cbec176b
Established class (EPC) Non-Standardized Chemical Allergen
Physiologic effect Increased Histamine Release; Cell-mediated Immunity; Increased IgG Production
Chemical class Allergens; Glycerol
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2015-07-14
Route TOPICAL
Dosage form SWAB
Substance GLYCERIN
Quick answers
  • RxCUI (RxNorm): 1114098
Why two NDCs? The FDA registers this code as 60913-061-03 — 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 → 60913-0061-03. 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 Non-Standardized Chemical Allergen class.

Pharmacologic class Non-Standardized Chemical Allergen
Drug family (ATC) Enemas, Other drugs for constipation
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.

Clinical

🧪 What is this product?

This is a topical swab stick containing glycerin, marketed as an over-the-counter monograph product. Glycerin is a humectant commonly used in oral care products to help moisturize and soothe the mouth and gums. The lemon flavoring in this product provides taste. These swabs are typically applied directly to the mouth or gums for localized comfort and moisture.

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.

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 eachPer 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.
Try another pack size: 50 pouches
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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
60913-0061-01 60913-061-01 Main listing 50 POUCH in 1 BOX / 1 PACKET in 1 POUCH / 1.4 g in 1 PACKET 2015-07-14 — Active
60913-0061-03 You're viewing this 25 POUCH in 1 BOX / 3 PACKET in 1 POUCH / 1.4 g in 1 PACKET 2015-07-14 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 25 pouch in 1 box / 3 packet in 1 pouch / 1.4 g in 1 packet.
What NDC number is used to bill for this package of Lemon Glycerine Swabsticks 7.5 g/100g Swab?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Lemon .3 g/4g 55681-0750-00 TwinMed 25 packets — — FDA listed —
Lemon Glycerine Swabsticks 7.5 g/100gthis 60913-0061-03 PHOENIX 25 pouches — — FDA listed —
Lemon Glycerin .3 g/4g 67777-0161-10 Dynarex 25 applicators — — FDA listed —
Lemon 7.5 mg/100mg 68786-0160-01 Sion 50 packets — — 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

🏛️
2015
On the market since
Jul 2015
📍
2026
Currently FDA-listed
11 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.

What it looks like

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 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

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

The official label also statesCitric acid, lemon flavor, sodium benzoate, water

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.

Manufacturer & labeler

LabelerPHOENIX HEALTHCARE SOLUTIONS, LLC
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code60913
First marketedJul 2015
Product typeHuman Otc Drug
Portfolio15 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.

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 21 words ▾

Uses For temporary relief of minor discomfort and protection of irritated areas in sore mouth and sore throat. Dry mouth relief.

⏱️ Dosage and Administration 33 words ▾

Directions: Swab mouth as needed Discard after single use. Children under the age of 12 should be supervised in the use of this product. Children under 2 years of age consult a doctor.

⚠️ Warnings 25 words ▾

Warnings For Oral Use Only. Do not use Do not get in eyes Keep out of reach of children Keep out of reach of children

📦 Storage and Handling 14 words ▾

Other information Store at room temperature: 15 C - 30 C Avoid excessive heat

🧪 Active Ingredient 5 words ▾

Active Ingredient Glycerin 7.5% v/v

🧪 Inactive Ingredients 9 words ▾

Inactive ingredients: Citric acid, lemon flavor, sodium benzoate, water

🎯 Purpose 3 words ▾

Purpose Oral Demulcent

📄 Do Not Use 8 words ▾

Do not use Do not get in eyes

📄 Keep Out of Reach of Children 12 words ▾

Keep out of reach of children Keep out of reach of children

📄 Package Label / Principal Display Panel 58 words ▾

Principal Display Panel NDC 60913-061-01 Phoenix Healthcare Solutions LLC "An Innovative Medical Manufacturer" Lemon-Glycerine Swabsticks For Professional and Hospital Use Antiseptic/Germicide 50 Pouches Per Box 1 Swabstick Per Pouch NDC 60913-061-03 Phoenix Healthcare Solutions LLC "An Innovative Medical Manufacturer" Lemon-Glycerine Swabsticks For Professional and Hospital Use Antiseptic/Germicide 25 Pouches Per Box 3 Swabstick Per Pouch Label Label 1

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

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 Glycerine — the ingredient across all brands.

Top reported reactions

Macular Degeneration123
Confusional State23
Cerebrovascular Accident21
Disorientation20
Speech Disorder20
Constipation19
Fatigue16

Age at onset

Infant2
Child1
Adolescent1
Adult10
Elderly8

Reporter sex

324 reports

Serious outcomes

Life-threatening33
Disabling1
Reports over time (by year) — tap or hover for the count & year
2020 2022 2024 2026 53 0
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.

About this NDC listing & data coverage

Over-the-counter (OTC) product
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.
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 form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
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 PHOENIX HEALTHCARE SOLUTIONS, LLC. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 50 pouches (60913-0061-01). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
PHOENIX HEALTHCARE SOLUTIONS, 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.
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.