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Antibacterial Foamy Mango High Foaming Antiseptic Hand and Body Wash CHLOROXYLENOL 3 mg/mL Soap, 18900 mL — NDC 60456-0876-19 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Antibacterial Foamy Mango High Foaming Antiseptic Hand and Body Wash CHLOROXYLENOL 3 mg/mL Soap, 18900 mL — NDC 60456-876-19 (Billing 60456-0876-19)

by Carpet Rentals, Inc. · 18900 mL in 1 CONTAINER

This is a package of 18,900 mL of Antibacterial Foamy Mango High Foaming Antiseptic Hand and Body Wash CHLOROXYLENOL 3 mg/mL Soap from Carpet Rentals, Inc., no longer marketed (first marketed Jan 2017), no longer in the FDA NDC Directory.

NDC 60456-0876-19
🏷️ FDA NDC (as labeled) 60456-876-19 billing pads the product segment with a zero
This package
Contains18900 mL Pack sizes23 compare ↓
Product page 60456-0876-01 Also comes in: 50 ml 60456-876-18 118 ml 60456-876-24 149 ml 60456-876-28 236 ml 60456-876-16 350 ml 60456-876-03 532 ml 60456-876-17 540 ml 60456-876-05 700 ml 60456-876-07 800 ml 60456-876-06 800 ml 60456-876-13 800 ml 60456-876-27 946 ml 60456-876-15 1000 ml 60456-876-08 1000 ml 60456-876-10 1000 ml 60456-876-11 1000 ml 60456-876-12 1200 ml 60456-876-01 2000 ml 60456-876-09 3785 ml 60456-876-14 75600 ml 60456-876-20 132500 ml 60456-876-35 208200 ml 60456-876-55
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ 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

⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. 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

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 60456-876-19
Product NDC 60456-876
11-digit billing NDC 60456087619
RxCUI 413261
UNII 0F32U78V2Q
Application # M003
SPL Set ID a95b4d71-119e-4c3b-a280-09bd4533252b
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm
Marketing start 2017-01-17
Route TOPICAL
Dosage form SOAP
Substance CHLOROXYLENOL
Quick answers
  • RxCUI (RxNorm): 413261
Why two NDCs? The FDA registers this code as 60456-876-19 — 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 → 60456-0876-19. 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 Phenol and derivatives class.

Drug family (ATC) Phenol and derivatives
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 an over-the-counter foaming hand and body wash that contains chloroxylenol, an antimicrobial agent. Chloroxylenol is typically used in topical products to help reduce bacteria and germs on the skin surface. This product is marketed as an OTC monograph drug, meaning it follows FDA's established safety and effectiveness standards for antiseptic hand and body wash products in this category. It is applied topically by washing hands or body with water.

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: 50 ml 118 ml 149 ml 236 ml 350 ml 532 ml 540 ml 700 ml 800 ml 800 ml 800 ml 946 ml 1000 ml 1000 ml 1000 ml 1000 ml 1200 ml 2000 ml 3785 ml 75600 ml 132500 ml 208200 ml
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
60456-0876-01 60456-876-01 Main listing 1200 mL in 1 CARTRIDGE 2017-01-17 — Discontinued by firm
60456-0876-03 60456-876-03 350 mL in 1 CARTRIDGE 2017-01-17 — Discontinued by firm
60456-0876-05 60456-876-05 540 mL in 1 BOTTLE, PLASTIC 2017-01-17 — Discontinued by firm
60456-0876-06 60456-876-06 1 BAG in 1 BOX / 800 mL in 1 BAG 2017-01-17 — Discontinued by firm
60456-0876-07 60456-876-07 700 mL in 1 BAG 2017-01-17 — Discontinued by firm
60456-0876-08 60456-876-08 1 BAG in 1 BOX / 1000 mL in 1 BAG 2017-01-17 — Discontinued by firm
60456-0876-09 60456-876-09 2000 mL in 1 CARTRIDGE 2017-01-17 — Discontinued by firm
60456-0876-10 60456-876-10 1000 mL in 1 CARTRIDGE 2017-01-17 — Active
60456-0876-11 60456-876-11 1000 mL in 1 BOTTLE, PLASTIC 2017-01-17 — Discontinued by firm
60456-0876-12 60456-876-12 1000 mL in 1 BAG 2017-01-17 — Discontinued by firm
60456-0876-13 60456-876-13 800 mL in 1 BAG 2017-01-17 — Discontinued by firm
60456-0876-14 60456-876-14 3785 mL in 1 BOTTLE, PLASTIC 2017-01-17 — Discontinued by firm
60456-0876-15 60456-876-15 946 mL in 1 BOTTLE, PLASTIC 2017-01-17 — Discontinued by firm
60456-0876-16 60456-876-16 236 mL in 1 BOTTLE, PLASTIC 2017-01-17 — Discontinued by firm
60456-0876-17 60456-876-17 532 mL in 1 BOTTLE, PLASTIC 2017-01-17 — Discontinued by firm
60456-0876-18 60456-876-18 50 mL in 1 BOTTLE, PLASTIC 2017-01-17 — Discontinued by firm
60456-0876-19 You're viewing this 18900 mL in 1 CONTAINER 2017-01-17 — Discontinued by firm
60456-0876-20 60456-876-20 75600 mL in 1 DRUM 2017-01-17 — Discontinued by firm
60456-0876-24 60456-876-24 118 mL in 1 BOTTLE, PLASTIC 2017-01-17 — Discontinued by firm
60456-0876-27 60456-876-27 800 mL in 1 CARTRIDGE 2017-01-17 — Discontinued by firm
60456-0876-28 60456-876-28 149 mL in 1 BOTTLE, PLASTIC 2017-01-17 — Discontinued by firm
60456-0876-35 60456-876-35 132500 mL in 1 DRUM 2017-01-17 — Discontinued by firm
60456-0876-55 60456-876-55 208200 mL in 1 DRUM 2017-01-17 — Discontinued by firm

Pack size FAQ

What quantity is in this package?
This package contains 18900 mL — 18900 ml in 1 container.
How does this package differ from NDC 60456-0876-18?
Both are Antibacterial Foamy Mango High Foaming Antiseptic Hand and Body Wash CHLOROXYLENOL 3 mg/mL Soap — the drug itself is identical. This page's package is the 18900 mL one, while NDC 60456-0876-18 is the 50 ml package.
What NDC number is used to bill for this package of Antibacterial Foamy Mango High Foaming Antiseptic Hand and Body Wash CHLOROXYLENOL 3 mg/mL Soap?
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 Drop Gentle Antiseptic 3 mg/mL 11429-1006-01 Woodbine 118 ml — — FDA listed —
Simplify Antibacterial Hand Apple Blossom Scent .3 g/100mL 11822-0281-01 Rite 573 ml — — Discontinued —
Antiseptic Hand 3 mg/mL 16496-0544-14 Image 3785 ml — — FDA listed —
Renown Antibacterial Hand 3000 mg/L 18949-0051-00 HD 3.78 l — — FDA listed —
Symmetry Antimicrobial Foaming Hand Wash .3 g/100mL 30805-0006-02 Buckeye 1250 ml — — FDA listed —
Altra Antimicrobial Foaming Hand Wash with 0.3% PCMX .3 g/100mL 30805-0016-02 Buckeye 1250 ml — — Discontinued —
Sentry Antiseptic Handsoap 3 mg/mL 31507-0544-14 Wechem, 3785 ml — — FDA listed —
Hand Guard High Foaming Antiseptic Hand and Body Wash 3 mg/mL 31507-0876-01 Wechem, 1200 ml — — Discontinued —
Chloroxylenol 0.30 % 3 mg/mL 42669-0028-03 Davion, 828 ml — — FDA listed —
Fm-24 Foaming 3 mg/mL 43097-0876-01 People's 1200 ml — — Discontinued —
Sani Foam Mango Antiseptic Hand and Body Wash 3 mg/mL 43374-0876-10 Delta 1000 ml — — Discontinued —
Pearl Antimicrobial Hand Item 1027Ab-01 .3 g/100mL 50536-0127-01 AMERICAN 3785 ml — — FDA listed —
Soft Touch Plus Antibacterial Hand Item 1039 .3 g/100mL 50536-0139-01 AMERICAN 3785 ml — — FDA listed —
Super Suds Antibacterial Hand Item 1063 .3 g/100mL 50536-0163-01 AMERICAN 3785 ml — — FDA listed —
E-2 Hand Item 1095 .3 g/100mL 50536-0195-01 AMERICAN 3785 ml — — FDA listed —
Golden Medicated .3 g/100mL 50865-0060-09 Kutol 3785 ml — — FDA listed —
Xtra Antibacterial Hand Juicy Orange 3 mg/mL 51628-0033-00 MY 709 ml — — FDA listed —
Ultra 3 mg/mL 55910-0589-44 Old 532 ml — — Discontinued —
Triclosan Free Antibacterial Antibacterial .3 g/100mL 57337-0086-01 Rejoice 443 ml — — FDA listed —
Triclosan Free Antibacterial 7.5 oz original Antibacterial .3 g/100mL 57337-0087-01 Rejoice 221 ml — — FDA listed —
Triclosan Free Antibacterial 7.5 oz (Ocean) Antibacterial .3 g/100mL 57337-0088-01 Rejoice 221 ml — — FDA listed —
Triclosan Free Antibacterial 7.5 oz (Strawberry Pomegranate) Antibacterial .3 g/100mL 57337-0089-01 Rejoice 221 ml — — FDA listed —
Triclosan Free Antibacterial 7.5 oz (Fresh Citrus) Antibacterial .3 g/100mL 57337-0090-01 Rejoice 221 ml — — FDA listed —
Chemseptic 3 mg/mL 59503-0544-01 Rochester 532 ml — — Discontinued —
Antibacterial Foamy Mango High Foaming Antiseptic Hand and Body Wash 3 mg/mLthis 60456-0876-19 Carpet 18900 ml — — Discontinued —
Franklin cleaning technology antibacterial hand 3 mg/mL 60933-0056-00 Fuller 3790 ml — — FDA listed —
1012 Antimicrobial 3 mg/mL 62257-0012-06 ABC 800 ml — — Discontinued —
Lynx Antibacterial 3 mg/mL 62257-0160-01 ABC 1200 ml — — Discontinued —
Lynx Foamy PCMX Antiseptic Hand and Body Wash 6876 3 mg/mL 62257-0161-01 ABC 1200 ml — — Discontinued —
LX0380 Lynx glacier fresh Antiseptic Hand and Body Wash 6380 3 mg/mL 62257-0380-12 ABC 1000 ml — — FDA listed —
Palm 3 mg/mL 62257-0544-06 ABC 800 ml — — FDA listed —
Lynx LX0864 peachy-foam antiseptic handsoap 3 mg/mL 62257-0686-12 ABC 1000 ml — — FDA listed —
Sani Mango Antiseptic Hand and Body Wash 3 mg/mL 62257-0875-01 ABC 1200 ml — — Discontinued —
Sani Mango Antiseptic Hand and Body Wash 3 mg/mL 62257-0876-01 ABC 1200 ml — — FDA listed —
Handtastic Foamy Mango Antiseptic Hand and Body Wash 3 mg/mL 63533-0876-01 Momar 1200 ml — — Discontinued —
Suds High Foaming Antiseptic Hand and Body Wash 3 mg/mL 63830-0876-01 Pro 1200 ml — — Discontinued —
Fresh Start 3 mg/mL 63830-0950-06 Pro 800 ml — — FDA listed —
Surgent Antiseptic 3 mg/mL 66155-0544-01 SunCoast 1200 ml — — Discontinued —
Zep Applaud AB .3 g/100mL 66949-0123-01 Zep 11400 ml — — FDA listed —
Inoderm Style Antibacterial 3 mg/.001L 73062-0055-00 Avro 3.8 l — — FDA listed —
Inoderm Choice Antibacterial 3 mg/mL 73062-0523-42 Avro 3800 ml — — FDA listed —
Kroger Antibacterial Green Apple Hand .3 g/100mL 73487-0001-01 Korex 709 ml — — Discontinued —
Power Force Antibacterial Handsoap Green Apple Scent .3 g/100mL 73487-0008-01 Korex 709 ml — — FDA listed —
Power Force Antibacterial Handsoap Citrus Scent .3 g/100mL 73487-0009-01 KOREX 709 ml — — FDA listed —
Freshands Premium Foamy Antibacterial Handsoap 6876 3 mg/mL 75632-0876-14 Consolidated 3785 ml — — Discontinued —
Satin Foam High Foaming Antiseptic Hand Wash 3 mg/mL 75990-0914-03 Certus 750 ml — — FDA listed —
Green Antibacterial Dish and HandSoap 30 mg/10mL 79481-0200-02 Meijer, 709 ml — — FDA listed —
TOTO Antibacterial Foam HandSoap 3 mg/mL 84791-0686-05 Toto 18927 ml — — FDA listed —
Ban-Aid 3 mg/mL 63830-0544-06 Pro 800 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

🏛️
2017
On the market since
Jan 2017
📍
2026
Currently FDA-listed
9 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.

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 3365R6427R
    A synthetic red dye derived from coal tar or petroleum. It colors the medicine red and helps make the tablet or capsule visually distinct for identification and branding purposes.
  • UNII ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • UNII Z17H97EA6Y
    A plant-derived mild cleanser made from natural sugars and oils. It acts as an emulsifier and surfactant to help mix water and oil-based ingredients together in the medicine.
  • UNII BYR0546TOW
    DMDM hydantoin is a preservative chemical used to prevent the growth of bacteria and fungi in medicines. It helps keep the product safe and stable throughout its shelf life.
  • UNII DEL7T5QRPN
    A synthetic preservative that kills bacteria and fungi. It's added to medications to prevent microbial growth and extend shelf life, especially in liquid or topical formulations.
  • UNII 229D0E1QFA
    Methylisothiazolinone is a synthetic chemical preservative that prevents bacterial and fungal growth in liquid medicines and topical products. It helps keep the medication safe and extends shelf life during storage.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • UNII BPV390UAP0
    Sodium laureth sulfate is a mild detergent and surfactant derived from coconut oil or petroleum. It helps mix oil and water in formulations and is often used as a cleaning or foaming agent in topical products like shampoos and cleansers.
  • 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.

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

The official label also stateswater, decyl glucoside, sodium laureth sulfate, cocamide MIPA, propylene glycol, DMDM hydantoin, fragrance, methylchloroisothiazolinone, methylisothiazolinone, aloe barbadensis, acid red 1

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

LabelerCarpet Rentals, Inc.
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code60456
First marketedJan 2017
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.

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 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 15 words ▾

Drug Facts Box OTC-Indications & Usage Section for hand-washing to decrease bacteria on the skin

⏱️ Dosage and Administration 28 words ▾

Drug Facts Box OTC-Dosage & Administration Section wet hands and forearms apply 5 milliliters (teaspoonful) or palmful to hands and forearms scrub thoroughly for 1 minute and rinse

⚠️ Warnings 9 words ▾

Drug Facts Box OTC-Warnings Section For external use only

🧪 Active Ingredient 8 words ▾

Drug Facts Box OTC-Active Ingredient Section Chloroxylenol 0.3%

🧪 Inactive Ingredients 26 words ▾

Drug Facts Box OTC-Inactive Ingredient Section water, decyl glucoside, sodium laureth sulfate, cocamide MIPA, propylene glycol, DMDM hydantoin, fragrance, methylchloroisothiazolinone, methylisothiazolinone, aloe barbadensis, acid red 1

🎯 Purpose 6 words ▾

Drug Facts Box OTC-Purpose Section Antiseptic

📄 When Using This Product 19 words ▾

Drug Facts Box OTC-When Using Section do not get into eyes if contact occurs, rinse eyes thoroughly with water

📄 Stop Use and Ask a Doctor If 10 words ▾

Drug Facts Box OTC-Stop Use Section irritation and redness develop

📄 Keep Out of Reach of Children 23 words ▾

Drug Facts Box OTC-Keep Out of Reach of Children Section if swallowed, get medical help or contact a Poison Control Center right away

📄 Package Label / Principal Display Panel 26 words ▾

Antibacterial Foamy Mango High Foaming Antiseptic Hand and Body Wash 6876 Label Antibacterial Foamy Mango High Foaming Antiseptic Hand and Body Wash 6876 Label product label

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

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 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.
Does this product come in other package sizes?
Yes — the FDA directory lists 22 other package presentations of this same product, including 50 ml (60456-0876-18), 118 ml (60456-0876-24), 149 ml (60456-0876-28). 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?
Carpet Rentals, 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.
← 60440-0961-01 · AstraZeneca 60468-0001-01 · allphamed →
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.