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Glycerin 1 g/1.25g Suppository, 1.2 g — NDC 13709-0333-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Glycerin 1 g/1.25g Suppository, 1.2 g — NDC 13709-333-01 (Billing 13709-0333-01)

by Neilmed Pharmaceuticals Inc. · 10 BLISTER PACK in 1 CARTON / 1.2 g in 1 BLISTER PACK

This is a package of 1.2 g of Glycerin 1 g/1.25g Suppository from Neilmed Pharmaceuticals Inc., marketed since Jun 2025 and currently FDA-listed. It is the main listing for this product, which comes in 2 package sizes.

NDC 13709-0333-01
🏷️ FDA NDC (as labeled) 13709-333-01 billing pads the product segment with a zero
This package
Contains1.2 g Pack sizes2 compare ↓
Main listing for product 13709-333 · Also comes in: 1.2 g 13709-333-02
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 →

This page is curated, coded, and maintained by

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

NDC database record

One package, one record: these facts belong to NDC 13709-333-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
13709 labeler · 333 product · 01 package
Package marketed since
Jun 11, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 1370933301 1
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 13709-333-01
Product NDC 13709-333
11-digit billing NDC 13709033301
RxCUI 252062
UNII PDC6A3C0OX
Application # M015
SPL Set ID 374a2ca3-ee04-09a7-e063-6394a90ab760
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 2025-06-11
Route RECTAL
Dosage form SUPPOSITORY
Substance GLYCERIN
Quick answers
  • RxCUI (RxNorm): 252062
Why two NDCs? The FDA registers this code as 13709-333-01 — 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 → 13709-0333-01. 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 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 rectal suppository containing glycerin as an active ingredient. Glycerin is commonly used in suppository form to help soften stool and draw water into the intestines, which typically makes bowel movements easier. This product is marketed as an over-the-counter medication under FDA's established rules for suppository products in this category, rather than as an individually reviewed drug application.

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.

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: 1.2 g
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
13709-0333-01 You're viewing this Main listing 10 BLISTER PACK in 1 CARTON / 1.2 g in 1 BLISTER PACK 2025-06-11 — Active
13709-0333-02 13709-333-02 25 BLISTER PACK in 1 JAR / 1.2 g in 1 BLISTER PACK 2026-05-07 — Active

Pack size FAQ

What quantity is in this package?
This package contains 1.2 g — 10 blister pack in 1 carton / 1.2 g in 1 blister pack.
How does this package differ from NDC 13709-0333-02?
Both are Glycerin 1 g/1.25g Suppository — the drug itself is identical. This page's package is the 1.2 g one, while NDC 13709-0333-02 is the 1 jar package.
What NDC number is used to bill for this package of Glycerin 1 g/1.25g Suppository?
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
Glycerin 1 g 70000-0429-01 Cardinal 25 suppositories $0.122 — Availability likely —
Glycerin 1 g 11822-3321-08 Rite 25 suppositories — — FDA listed —
Rite-Aid Childrens Glycerin Laxative 1 g 11822-9101-02 RITE 25 suppositories — — FDA listed —
Glycerin 1 g/1.25gthis 13709-0333-01 Neilmed 1.2 g — — FDA listed —
Glycerin 1 g 37808-0399-25 H 25 suppositories — — FDA listed —
Stratuscare Glycerin Laxative Pediatric 1 g 58980-0409-12 Stratus 12 suppositories — — FDA listed —
Glycerin 1 g 68016-0161-00 Chain 25 suppositories — — FDA listed —
Glycerin 1 g/1.21 69842-0722-25 CVS 25 suppositories — — 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

🏛️
2025
On the market since
Jun 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.

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 55X04QC32I
    A strong alkaline chemical used to adjust and maintain the pH balance of liquid medicines. It helps keep the medicine stable and ensures it stays effective during storage.
  • UNII 4ELV7Z65AP
    Stearic acid is a fatty acid derived from plant or animal sources. It acts as a binder and lubricant in tablets and capsules, helping them hold together and flow smoothly during manufacturing.
  • 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 statesPurified water, sodium hydroxide, stearic acid

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

LabelerNeilmed Pharmaceuticals Inc.
FDA applicationM015 (OTC MONOGRAPH DRUG)
Labeler code13709
First marketedJun 2025
Product typeHuman Otc Drug
Portfolio25 products on file

More NDCs from Neilmed Pharmaceuticals Inc. labeler code 13709

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 ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 Ask a Doctor Before Use If 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 16 words ▾

Uses • relieves occasional constipation (irregularity) • generally, produces bowel movement in ¼ to 1 hour

⏱️ Dosage and Administration 47 words ▾

Directions Children 2 to under 6 years 1 suppository per day or as directed by a doctor Children under 2 years Ask a doctor Insert 1 suppository well into the rectum. To produce laxative action, suppository is designed to dissolve only partially and may not be noticeable

⚠️ Warnings 5 words ▾

Warnings For rectal use only

🧪 Active Ingredient 8 words ▾

Active Ingredient(in each suppository) Glycerin, USP 1 grams

🧪 Inactive Ingredients 6 words ▾

Purified water, sodium hydroxide, stearic acid

🎯 Purpose 2 words ▾

Purpose Laxative

📄 Do Not Use 15 words ▾

Do not use laxative products for longer than 1 week unless directed by a doctor

📄 Ask a Doctor Before Use If 28 words ▾

Ask a doctor before use if you have • stomach pain • nausea • vomiting • noticed a sudden change in bowel habits that lasts over 2 weeks

📄 When Using This Product 14 words ▾

When using this product, your child may have rectal discomfort or a burning sensation

📄 Stop Use and Ask a Doctor If 32 words ▾

Stop use and ask a doctor if your child has rectal bleeding or fails to have a bowel movement after use of a laxative. These could be signs of a serious condition.

📄 Keep Out of Reach of Children 20 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

📄 Other Information 56 words ▾

Other information • Store at room temperature. Do not exceed 30˚ C (86˚ F) • Lot No. & Exp. Date: see wrapper or box

Important: Please do not discard this printed box and any enclosed printed material. The inside final product may not have all the details you require for the ongoing use of the product.

📄 Questions or Comments 5 words ▾

Questions or comments? 1(877) 477-8633

📄 Package Label / Principal Display Panel 3 words ▾

Children Glycerin Suppository

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 Glycerin (this brand).

Top reported reactions

Macular Degeneration598
Constipation447
Pain404
Nausea329
Pyrexia314
Malaise277
Weight Decreased270

Age at onset

Neonate3
Infant9
Child11
Adolescent7
Adult149
Elderly330

Reporter sex

2,678 reports
Male · 34%
Female · 66%
Unknown · 0%

Serious outcomes

Hospitalization1,469
Death378
Life-threatening293
Disabling52
Reports over time (by year) — tap or hover for the count & year
2020 2022 2024 2026 479 100
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 Neilmed Pharmaceuticals Inc.. 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 1 jar (13709-0333-02). 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?
Neilmed 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.
← 13709-0332-01 · NeilMed 13709-0334-01 · Neilmed →
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.