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GoodSense Eye Drops Advanced Relief Moisturizer dextran, polyethylene glycol 400, povidone, tetrahydrozoline HCl 400 1 g/100mL; .05 g/100mL; 1 g/100mL; 70 .1 g/100mL Solution, 15 mL — NDC 68788-8635-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

GoodSense Eye Drops Advanced Relief Moisturizer dextran, polyethylene glycol 400, povidone, tetrahydrozoline HCl 400 1 g/100mL; .05 g/100mL; 1 g/100mL; 70 .1 g/100mL Solution, 15 mL — NDC 68788-8635-1 (Billing 68788-8635-01)

by Preferred PHarmaceuticals Inc. · 1 CARTON in 1 CARTON / 15 mL in 1 CARTON

This is a package of 15 mL of GoodSense Eye Drops Advanced Relief Moisturizer dextran, polyethylene glycol 400, povidone, tetrahydrozoline HCl 400 1 g/100mL; .05 g/100mL; 1 g/100mL; 70 .1 g/100mL Solution from Preferred PHarmaceuticals Inc., marketed since Apr 2024 and currently FDA-listed. It is this product's only package size.

NDC 68788-8635-01
🏷️ FDA NDC (as labeled) 68788-8635-1 billing pads the package segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Aug 27, 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 68788-8635-1 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
68788 labeler · 8635 product · 1 package
Package marketed since
Apr 16, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Billing quantity
15 mL per package
Barcode (UPC-A, from the NDC)
3 6878886351 5
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 68788-8635-1
Product NDC 68788-8635
11-digit billing NDC 68788863501
NCPDP billing unit ML — per mL (volume)
RxCUI 996202
UNII B697894SGQ, 0YZT43HS7D, FZ989GH94E, 7SA290YK68
Application # M018
SPL Set ID 011473a8-26d5-4661-b3c0-745f9b6aa1d8
Established class (EPC) Plasma Volume Expander
Mechanism of action Osmotic Activity
Physiologic effect Increased Intravascular Volume
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-04-16
Route OPHTHALMIC
Dosage form SOLUTION
Substance POLYETHYLENE GLYCOL 400; TETRAHYDROZOLINE HYDROCHLORIDE; POVIDONE, UNSPECIFIED; DEXTRAN 70
Quick answers
  • RxCUI (RxNorm): 996202
Why two NDCs? The FDA registers this code as 68788-8635-1 — 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 → 68788-8635-01. 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 Plasma Volume Expander class.

Pharmacologic class Plasma Volume Expander
How it works Osmotic Activity
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

📖 About the active ingredient MedlinePlus · NLM
General information about the ingredient itself — the description of this specific product follows below.

Ophthalmic tetrahydrozoline is used to relieve minor eye irritation and redness caused by colds, pollen, and swimming.

Read the full MedlinePlus article ↗
🧪 What is this product?

GoodSense Eye Drops Advanced Relief Moisturizer is an over-the-counter eye drop solution regulated under FDA's OTC monograph rules for ophthalmic decongestants and lubricants. It contains tetrahydrozoline hydrochloride, a decongestant typically used to reduce redness and relieve minor eye irritation. The other ingredients (dextran 70, polyethylene glycol 400, and povidone) function as lubricants and moisture-retention agents commonly used to soothe dry or irritated eyes.

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 mLPer 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
68788-8635-01 You're viewing this Main listing 1 CARTON in 1 CARTON / 15 mL in 1 CARTON 2024-04-16 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Leader Advanced Relief Eye Drops 70 100 mg/100mL; 400 1000 mg/100mL; 1000 mg/100mL; 50 mg/100mL 70000-0456-01 Cardinal 1 bottle $0.152 — Availability likely —
Quality Choice Moisturizing Relief Eye Drops 70 .1 g/100mL; .05 g/100mL; 1 g/100mL; 400 1 g/100mL 83324-0191-14 Chain 1 bottle $0.152 — Availability likely —
Sunmark Eye Drops Advanced Moisturizer/Lubricant 70 .1 g/100mL; 400 1 g/100mL; 1 g/100mL; .05 g/100mL 49348-0697-29 Strategic 1 bottle $0.154 — FDA listed —
Walgreens Eye Drops Advanced Relief 15mL 70 .1 g/100mL; 400 1 g/100mL; 1 g/100mL; .05 g/100mL 00363-4547-01 Walgreen 1 bottle — — FDA listed —
Signature Care Eye Drops Advanced Relief 70 100 mg/100mL; 400 1000 mg/100mL; 1000 mg/100mL; 50 mg/100mL 21130-0704-01 Better 1 bottle — — FDA listed —
Kroger Eye Drops Advanced Relief 70 .1 g/100mL; 400 1 g/100mL; 1 g/100mL; .05 g/100mL 30142-0836-01 Kroger 1 bottle — — FDA listed —
TopCare Health Advanced Moisturizing Plus Redness Relief 1 g/100mL; .05 g/100mL; 400 1 g/100mL; 70 .1 g/100mL 36800-0856-01 Topco 1 bottle — — FDA listed —
HEB Advanced Eye Drops 70 .1 g/100mL; 400 1 g/100mL; 1 g/100mL; .05 g/100mL 37808-0786-01 HEB 1 bottle — — FDA listed —
Equaline Advanced Relief Eye Drops 70 .1 g/100mL; 400 1 g/100mL; 1 g/100mL; .05 g/100mL 41163-0338-01 United 1 bottle — — FDA listed —
Meijer Advanced Redness and Irritation Relief 400 1 g/100mL; .05 g/100mL; 70 .1 g/100mL; 1 g/100mL 41250-0594-01 Meijer 1 bottle — — FDA listed —
GoodSense Eye Drops Advanced Relief Moisturizer 400 1 g/100mL; .05 g/100mL; 1 g/100mL; 70 .1 g/100mL 50804-0130-01 Geiss, 15 ml — — FDA listed —
CVS Advanced Eye Drops 70 .1 g/100mL; 400 1 g/100mL; 1 g/100mL; .05 g/100mL 51316-0129-01 CVS 1 bottle — — FDA listed —
Discount Drug Mart Eye Drops Advanced Relief 70 .1 g/100mL; 400 1 g/100mL; 1 g/100mL; .05 g/100mL 53943-0422-01 Discount 1 bottle — — FDA listed —
Exchange Select Eye Drops Advanced Relief Moisturizer 400 1 g/100mL; .05 g/100mL; 1 g/100mL; 70 .1 g/100mL 55301-0177-01 Army 1 bottle — — FDA listed —
Medics Choice Eye Drops Advanced 10 mg/mL; 400 10 mg/mL; .5 mg/mL; 70 1 mg/mL 55651-0025-01 KC 1 bottle — — FDA listed —
DG Health Advanced Relief Eye Drops 1 g/100mL; 70 .1 g/100mL; .05 g/100mL; 400 1 g/100mL 55910-0361-01 Dolgencorp 1 bottle — — FDA listed —
Publix Advanced Relief Eye Drops 70 .1 g/100mL; 400 1 g/100mL; 1 g/100mL; .05 g/100mL 56062-0084-01 Publix 1 bottle — — FDA listed —
Core Values Eye Drops Advanced Relief 70 .1 g/100mL; 400 1 g/100mL; 1 g/100mL; .05 g/100mL 63940-0344-01 Liberty 1 bottle — — FDA listed —
Best Choice Eye Drops Advanced Relief 70 .1 g/100mL; 400 1 g/100mL; 1 g/100mL; .05 g/100mL 63941-0942-15 Valu 1 bottle — — FDA listed —
Winco Advanced Relief Eye Drops 70 100 mg/100mL; 400 1000 mg/100mL; 1000 mg/100mL; 50 mg/100mL 67091-0282-15 WinCo 1 bottle — — FDA listed —
GoodSense Eye Drops Advanced Relief Moisturizer 400 1 g/100mL; .05 g/100mL; 1 g/100mL; 70 .1 g/100mLthis 68788-8635-01 Preferred 15 ml — — FDA listed —
Harris Teeter Eye Drops Advanced Relief 70 .1 g/100mL; 400 1 g/100mL; 1 g/100mL; .05 g/100mL 69256-0662-01 Harris 1 bottle — — FDA listed —
GoodSense Eye Drops Advanced Relief Moisturizer 400 1 g/100mL; .05 g/100mL; 1 g/100mL; 70 .1 g/100mL 85766-0165-15 Sportpharm 15 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

🏛️
2024
On the market since
Apr 2024
📍
2026
Currently FDA-listed
2 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 F5UM2KM3W7
    Benzalkonium chloride is a chemical compound that works as a preservative and antimicrobial agent in medications. It prevents bacterial and fungal growth in liquid formulations to keep the product safe during storage and use.
  • UNII R57ZHV85D4
    Boric acid is a weak acid derived from boron. In medicines, it typically serves as a buffer to help maintain the product's pH level and may act as a preservative in certain formulations.
  • UNII 7FLD91C86K
    Edetate disodium is a chemical compound that binds and removes certain metal ions. In medicines, it acts as a preservative and stabilizer by preventing metals like calcium from interfering with the product's shelf life and consistency.
  • UNII 91MBZ8H3QO
    Sodium borate is an inorganic salt compound used in medicines as a buffer to help maintain a stable pH level, and sometimes as a mild preservative or cleansing agent in topical formulations.
  • UNII 451W47IQ8X
    Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.
  • 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.

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

The official label also statesInactive ingredients benzalkonium chloride, boric acid, edetate disodium, purified water, sodium borate, and sodium chloride

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

LabelerPreferred PHarmaceuticals Inc.
FDA applicationM018 (OTC MONOGRAPH DRUG)
Labeler code68788
First marketedApr 2024
Product typeHuman Otc Drug
Portfolio833 products on file

More NDCs from Preferred PHarmaceuticals Inc. labeler code 68788

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 📄 Ask a Doctor Before Use If 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 27 words ▾

Uses • relieves redness of the eye due to minor eye irritations • as a lubricant to prevent further irritation or to relieve dryness of the eye

⏱️ Dosage and Administration 22 words ▾

Directions Instill 1 to 2 drops in the affected eye(s) up to 4 times daily. Relabeled By: Preferred Pharmaceuticals Inc. NDC 68788-8635-1

⚠️ Warnings 136 words ▾

Warnings For external use only Ask a doctor before use if you have narrow angle glaucoma 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 When using this product • pupils may become enlarged temporarily • to avoid contamination, do not touch tip of container to any surface. Replace cap after using. • if solution changed color or becomes cloudy, do not use • overuse may produce increased redness of the eye • remove contact lens before using If pregnant or breast-feeding , ask a health professional before use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison control Center (1-800-111-1222) right away.

🧪 Active Ingredient 10 words ▾

Active Ingredients Dextran 70.....0.1% Polyethylene glycol 400.....1% Povidone.....1% tetrahydrozoline HCl.....0.05%

🧪 Inactive Ingredients 15 words ▾

Inactive ingredients benzalkonium chloride, boric acid, edetate disodium, purified water, sodium borate, and sodium chloride

🎯 Purpose 11 words ▾

Purposes Dextran 70.....Lubricant Polyethylene glycol 400.....Lubricant Povidone.....Lubricant Tetrahydrozoline HCl .....Redness reliever

📄 Ask a Doctor Before Use If 11 words ▾

Ask a doctor before use if you have narrow angle glaucoma

📄 When Using This Product 53 words ▾

When using this product • pupils may become enlarged temporarily • to avoid contamination, do not touch tip of container to any surface. Replace cap after using. • if solution changed color or becomes cloudy, do not use • overuse may produce increased redness of the eye • remove contact lens before using

📄 Stop Use and Ask a Doctor If 36 words ▾

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

🤰 If Pregnant or Breast-Feeding 11 words ▾

If pregnant or breast-feeding , ask a health professional before use.

📄 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 (1-800-111-1222) right away.

📄 Package Label / Principal Display Panel 5 words ▾

Eye Drops Advanced Relief Moisturizer

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
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 Preferred PHarmaceuticals Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Preferred 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.
← 68788-8634-01 · Preferred 68788-8636-01 · Preferrred →
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.