Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.
REFRESH TEARS Carboxymethylcellulose sodium Kit — NDC 0023-0795-65 (Billing 00023-0795-65)
by Allergan, Inc. · 1 TRAY in 1 CARTON / 1 KIT in 1 TRAY * 15 mL in 1 BOTTLE, DROPPER * 5 mL in 1 BOTTLE, DROPPER
This is a package of REFRESH TEARS Carboxymethylcellulose sodium Kit from Allergan, Inc., marketed since Jan 2000 and currently FDA-listed. It is this product's only package size.
NDC 00023-0795-65
🏷️ FDA NDC (as labeled)
0023-0795-65
billing pads the labeler segment with a zero
🗂️ 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 →
⚠️
Other active recalls for Carboxymethylcellulose Sodium (different manufacturers) — 6 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Apr 23, 2025 — cGMP deviations and lack of assurance of sterility. (BRS Analytical Services, LLC) · FDA recall D-0406-2025
Class III · Dec 18, 2024 — LABELING: LABEL MIX-UP (AvKARE) · FDA recall D-0175-2025
Class I · Nov 13, 2023 — Non-Sterility (Kilitch Healthcare India Limited) · FDA recall D-0291-2024
Class I · Nov 13, 2023 — Non-Sterility (Kilitch Healthcare India Limited) · FDA recall D-0299-2024
Class I · Oct 31, 2023 — Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility. (Cardinal Health Inc.) · FDA recall D-0134-2024
Class I · Oct 31, 2023 — Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility. (Cardinal Health Inc.) · FDA recall D-0132-2024
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
0023-0795-65
Product NDC
0023-0795
11-digit billing NDC
00023079565
RxCUI
1188426
UNII
K679OBS311
Application #
M018
SPL Set ID
329d1fe0-4432-4565-b7b1-65666bd86526
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2000-01-01
Dosage form
KIT
Quick answers
- RxCUI (RxNorm): 1188426
Why two NDCs?
The FDA registers this code as 0023-0795-65 — a 4-4-2 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 labeler segment → 00023-0795-65. 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
Clinical
🧪 What is this product?
Refresh Tears is an over-the-counter eye lubricant kit containing carboxymethylcellulose sodium, a thick liquid that functions as an artificial tear substitute. This ingredient is commonly used to coat and moisten the eye surface, helping to relieve dryness and irritation. Carboxymethylcellulose sodium works by forming a protective film that keeps moisture on the eye longer than natural tears alone. This product is marketed under FDA's over-the-counter monograph rules for eye lubricants.
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.
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
💬 Questions about Carboxymethylcellulose sodium?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
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.
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 3, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 00023-0795-65 You're viewing this Main listing | 1 TRAY in 1 CARTON / 1 KIT in 1 TRAY * 15 mL in 1 BOTTLE, DROPPER * 5 mL in 1 BOTTLE, DROPPER | 2000-01-01 | — | Active |
Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Leader Lubricant Eye Drops .5 g/100mL 70000-0012-01 | Cardinal | 70 vials | $0.163 | — | Availability likely | — |
| Rugby Lubricant Eye Drops .5 g/100mL 00536-1387-92 | Rugby | 30 vials | $0.227 | — | Availability likely | — |
| Good Neighbor Pharmacy Lubricant Eye Drops .5 g/100mL 46122-0756-56 | Amerisource | 30 vials | $0.227 | — | Availability likely | — |
| carboxymethylcellulose sodium 5 mg/mL 50268-0067-30 | AvPAK | 30 vials | $0.227 | — | Availability likely | — |
| Foster and Thrive Lubricant Eye Drops .5 g/100mL 70677-1190-01 | Strategic | 30 vials | $0.227 | — | Availability likely | — |
| Carboxymethylcellulose Sodium Eye Lubricant 5 mg/mL 42494-0448-05 | Cameron | 2 bottles | $0.275 | — | Discontinued | — |
| Rugby Carboxymethylcellulose Sodium 0.5% Eye Drops .5 g/100mL 00536-1386-35 | Rugby | 2 bottles | $0.280 | — | Availability likely | — |
| carboxymethylcellulose sodium 5 mg/mL 50268-0068-15 | AvPAK | 1 bottle | $0.324 | — | Availability likely | — |
| Leader Lubricant Eye Drops Soothing Relief .5 g/100mL 70000-0705-01 | LEADER/Cardinal | 1 bottle | $0.324 | — | Availability likely | — |
| Refresh Tears 5 mg/mL 00023-0798-01 | Allergan, | 2 bottles | $0.412 | — | Availability likely | — |
| Lubricant Drops 5 mg/mL 70000-0090-01 | CARDINAL | 1 bottle | $0.498 | — | FDA listed | — |
| Refresh Plus 5 mg/mL 00023-0403-05 | Allergan, | 5 vials | — | — | FDA listed | — |
| Refresh Tearsthis 00023-0795-65 | Allergan, | 1 kit | — | — | FDA listed | — |
| Walgreens Lubricant Eye Drops Preservative Free .5 g/100mL 00363-8800-01 | Walgreen | 30 vials | — | — | FDA listed | — |
| Walgreens Lubricant Eye Drops 5 mg/mL 00363-8832-15 | Walgreen | 2 bottles | — | — | FDA listed | — |
| Walgreens Lubricant Eye Drops 5 mg/mL 00363-8833-15 | Walgreen | 1 bottle | — | — | FDA listed | — |
| Lubricant Eye 5 mg/mL 00536-1476-92 | Rugby | 30 ampules | — | — | FDA listed | — |
| Lubricant Eye Drops Preservative Free .5 g/100mL 11673-0150-01 | Target | 70 vials | — | — | FDA listed | — |
| Up and Up Dry Eye Relief Lubricant Eye Drops 5 mg/mL 11673-0771-01 | Target | 2 bottles | — | — | FDA listed | — |
| Up and Up Dry Eye Relief Lubricant Eye Drops 5 mg/mL 11716-0771-01 | Hanlim | 2 bottles | — | — | FDA listed | — |
| Auro-Cmc 5 mg/mL 16030-0401-10 | Aurolab | 10 ml | — | — | FDA listed | — |
| Carboxymethylcellulose Sodium Eye Drops 0.5% 5 mg/mL 16030-0501-05 | Aurolab | 5 ml | — | — | FDA listed | — |
| Gentle Eyes Lubricant Eye Drops 5 mg/mL 17312-0430-15 | TRP | 1 bottle | — | — | FDA listed | — |
| Signature Care Lubricant Eye Drops .5 g/100mL 21130-0705-01 | Better | 30 vials | — | — | FDA listed | — |
| Kroger Lubricant Eye .5 g/100mL 30142-0373-33 | The | 30 vials | — | — | FDA listed | — |
| HEB Lubricant Eye Drops .5 g/100mL 37808-0100-01 | HEB | 30 vials | — | — | FDA listed | — |
| Medi-First Lubricant Eye Drops .5 g/100mL 47682-0193-83 | Unifirst | 30 ampules | — | — | FDA listed | — |
| Green Guard Lubricant Eye Drops .5 g/100mL 47682-0194-83 | UniFirst | 30 ampules | — | — | FDA listed | — |
| Equate Lubricant Eye Drops Preservative-Free .5 g/100mL 49035-0245-01 | Wal-Mart | 25 vials | — | — | FDA listed | — |
| Equate Restore Plus Lubricant Eye Drops .5 g/100mL 49035-0389-01 | Walmart, | 70 vials | — | — | FDA listed | — |
| Good Sense Lubricating Plus Lubricant Eye Drops .5 g/100mL 50804-0700-01 | GoodSense | 30 bottles | — | — | FDA listed | — |
| Carboxymethylcellulose Sodium 0.5% 5 mg/mL 51407-0945-30 | Golden | 3 pouches | — | — | Discontinued | — |
| Discount Drug Mart Lubricant Eye Drops 5 mg/mL 53943-0510-01 | Discount | 5 bottles | — | — | FDA listed | — |
| Retaine CMC 5 mg/mL 54799-0460-30 | OCuSOFT | 30 vials | — | — | FDA listed | — |
| Medics Choice Lubricant Eye Drops .5 g/100mL 55651-0030-01 | K.C. | 5 ampules | — | — | FDA listed | — |
| Lubricant Eye Drops 5 mg/mL 55651-0105-05 | KC | 5 bottles | — | — | FDA listed | — |
| Lubricant Eye Drops 5 mg/mL 55651-0510-01 | KC | 5 bottles | — | — | FDA listed | — |
| Publix Moisturizing Relief Eye Drops .5 g/100mL 56062-0789-01 | Publix | 30 vials | — | — | FDA listed | — |
| TheraTears Dry and Tired 5 mg/mL 58790-0013-30 | MEDTECH | 6 pouches | — | — | FDA listed | — |
| Family Care Single Use Lubricant Eye Drop 0.4mL 5ct 5 mg/mL 65923-0575-05 | United | 1 vial | — | — | FDA listed | — |
| Family Care Single Use Lubricant Eye Drop 0.4mL 30ct 5 mg/mL 65923-0576-30 | United | 30 vials | — | — | FDA listed | — |
| Refresh Tears 5 mg/mL 66715-1073-00 | Lil' | 1 bottle | — | — | Discontinued | — |
| Refresh Tears Lubricant 5 mg/mL 67751-0130-01 | Navajo | 3 ml | — | — | Discontinued | — |
| Lubricating Tears 5 mg/mL 69618-0076-55 | Reliable | 1 bottle | — | — | FDA listed | — |
| CVS Lubricant Eye Drops .5 g/100mL 69842-0804-01 | CVS | 70 vials | — | — | FDA listed | — |
| CVS Lubricant Eye Drops 30 ct .5 g/100mL 69842-0993-01 | CVS | 30 vials | — | — | FDA listed | — |
| Lubricant Eye 5 mg/mL 70000-0751-01 | CARDINAL | 30 ampules | — | — | FDA listed | — |
| Lubricant Eye Drops 5 mg/mL 71105-0105-05 | Redicare | 5 bottles | — | — | FDA listed | — |
| TopCare Health Lubricant Eye Drops .5 g/100mL 76162-0089-30 | Topcare | 30 vials | — | — | FDA listed | — |
| Meijer Lubricant Eye Drops .5 g/100mL 79481-0066-01 | Meijer | 30 vials | — | — | FDA listed | — |
| Rain Renewal Eye Drops .5 g/100mL 79662-0001-30 | Rain | 30 bottles | — | — | FDA listed | — |
| Equate Moisturizing Comfort Lubricant Eye Drops .5 g/100mL 79903-0264-05 | Walmart | 1 bottle | — | — | FDA listed | — |
| Focus Tears PF 5 mg/mL 82724-0009-20 | Covalent | 30 vials | — | — | FDA listed | — |
| Eyes Alive Lubricating 5 mg/mL 83291-0200-00 | RIVIERA | 100 ampules | — | — | 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Sep 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2000
On the market since
Jan 2000
📍
2026
Currently FDA-listed
26 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.
- FDA Orange Book · refreshed Sep 3, 2026
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.
From the label’s inactive-ingredient sectionBoric acid; calcium chloride dihydrate; magnesium chloride hexahydrate; potassium chloride; purified water; PURITE ® (stabilized oxychloro complex); sodium borate decahydrate; and sodium chloride. May contain hydrochloric acid and/or sodium hydroxide (to adjust pH).
This is label-wide narrative text, not a normalized exact-product ingredient list. A label can cover multiple strengths or packages.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured
IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.- FDA label on DailyMed · label index refreshed Oct 1, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
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
LabelerAllergan, Inc.
FDA applicationM018 (OTC MONOGRAPH DRUG)
Labeler code00023
First marketedJan 2000
Product typeHuman Otc Drug
Portfolio188 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 openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
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
📄 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 ▾
Uses For the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun. May be used as a protectant against further irritation.
⏱️ Dosage and Administration ▾
Directions Instill 1 or 2 drops in the affected eye(s) as needed.
⚠️ Warnings ▾
Warnings For external use only. To avoid contamination, do not touch tip of container to any surface. Replace cap after using.
If solution changes color or becomes cloudy, do not use. Stop use and ask a doctor if you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours. Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
🧪 Active Ingredient ▾
Active ingredient Carboxymethylcellulose sodium 0.5%
🧪 Inactive Ingredients ▾
Inactive ingredients Boric acid; calcium chloride dihydrate; magnesium chloride hexahydrate; potassium chloride; purified water; PURITE ® (stabilized oxychloro complex); sodium borate decahydrate; and sodium chloride. May contain hydrochloric acid and/or sodium hydroxide (to adjust pH).
🎯 Purpose ▾
Purpose Eye lubricant
📄 Stop Use and Ask a Doctor If ▾
Stop use and ask a doctor if you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours.
📄 Keep Out of Reach of Children ▾
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
📄 Other Information ▾
Other information Use only if tape seals on top and bottom flaps are intact. Use before expiration date marked on container. Discard 90 days after opening. Store at 59°-77°F (15°-25°C). RETAIN THIS CARTON FOR FUTURE REFERENCE.
📄 Questions or Comments ▾
Questions or comments? 1.800. 6 78 . 1605 refreshbrand.com v1.0DFL0798
📄 Package Label / Principal Display Panel ▾
PRINCIPAL DISPLAY PANEL Refresh Tears ® Lubricant Eye Drops ORIGINAL STRENGTH Moisturizing Relief for Dry, Irritated Eyes 0.5 fl oz (15 mL) Sterile Refresh Tears® Lubricant Eye Drops ORIGINAL STRENGTH Moisturizing Relief for Dry, Irritated Eyes 0.5 fl oz (15 mL) Sterile
PRINCIPAL DISPLAY PANEL Multi-Pack More bottles for more places Refresh Tears ® Lubricant Eye Drops ORIGINAL STRENGTH Moisturizing Relief for Dry, Irritated Eyes 4 bottles 0.5 fl oz (15 mL) each plus 1 bottle 0.17 fl oz (5 mL) Sterile Multi-Pack More bottles for more places Refresh Tears® Lubricant Eye Drops ORIGINAL STRENGTH Moisturizing Relief for Dry, Irritated Eyes 4 bottles 0.5 fl oz (15 mL) each plus 1 bottle 0.17 fl oz (5 mL) Sterile
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 ↗
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 Refresh Tears (this brand).
Top reported reactions
Age at onset
Reporter sex
Male · 23%
Female · 76%
Unknown · 0%
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.
About this NDC listing & data coverage
Over-the-counter (OTC) product
Kit / multi-component package
Kit / multi-component package
This NDC identifies a kit — a package containing more than one component. Structured data (pricing, ingredients, equivalents) is often reported per component rather than for the kit NDC itself, which can make this page look thinner than the components' own pages.
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 Allergan, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Allergan, 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.
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.