Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.
PATADAY ONCE DAILY RELIEF OLOPATADINE HYDROCHLORIDE 2 mg/mL Solution, 3 bottles — NDC 0065-8150-07 (Billing 00065-8150-07)
by Alcon Laboratories, Inc. · 3 BOTTLE, PLASTIC in 1 CARTON / 2.5 mL in 1 BOTTLE, PLASTIC
This is a package of 3 bottles of PATADAY ONCE DAILY RELIEF OLOPATADINE HYDROCHLORIDE 2 mg/mL Solution from Alcon Laboratories, Inc., marketed since Feb 2020 and currently FDA-listed.
NDC 00065-8150-07
🏷️ FDA NDC (as labeled)
0065-8150-07
billing pads the labeler segment with a zero
This package
Contains3 bottles
Pack sizes4 compare ↓
Product page 00065-8150-01
Also comes in:
2.5 mL 0065-8150-01
1 bottle 0065-8150-04
2 bottles 0065-8150-03
🗂️ 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 →
Past resolved recalls for this product (1)
Class II · Jun 29, 2022 · Terminated — CGMP Deviations: products were stored outside the drug label specifications. (Mckesson Medical-Surgical Inc. Corporate Office) · FDA recall D-1321-2022
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
0065-8150-07
Product NDC
0065-8150
11-digit billing NDC
00065815007
UNII
2XG66W44KF
Application #
NDA021545
SPL Set ID
1c7d2342-ba1c-4244-9814-d92a05725d4e
Established class (EPC)
Histamine-1 Receptor Antagonist; Histamine-1 Receptor Inhibitor; Mast Cell Stabilizer
Mechanism of action
Histamine H1 Receptor Antagonists
Physiologic effect
Decreased Histamine Release
DEA schedule
Non-controlled
Marketing category
NDA
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2020-02-28
Route
OPHTHALMIC
Dosage form
SOLUTION
Substance
OLOPATADINE HYDROCHLORIDE
Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification
GPI-14
86802065102030
GPI class
Pataday
GCN Seq No
062065
GCN
97848
HICL code
012815
Ingredient (HICL)
Olopatadine Hcl
HIC1 code
Q
Therapeutic class — broad (HIC1)
Ear/Eye/Nose/Rectum/Topical/Vagina/Other
HIC2 code
Q6
Therapeutic class — intermediate (HIC2)
Ophthalmic Preparations
HIC3 code
Q6R
Therapeutic class — specific (HIC3)
Eye Antihistamines
AHFS code
52:02.00.00
AHFS class
Antiallergic Agents
FDB label name
PATADAY ONCE DAILY 0.2% DROPS
FDB brand name
Pataday Once Daily Relief
Legend status
O — Over-the-counter (OTC) drug or device
Quick answers
- GSN (GCN sequence number): 062065
- GCN: 97848
- GPI-14 (Medi-Span): 86802065102030
- HICL (First Databank): 012815
- AHFS class code: 52:02.00.00
- RxCUI (RxNorm): 1111343
Why two NDCs?
The FDA registers this code as 0065-8150-07 — 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 → 00065-8150-07. 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
RxNorm drug class
This medicine belongs to the Histamine-1 Receptor Inhibitor class.
Pharmacologic class
Histamine-1 Receptor Inhibitor, Histamine-1 Receptor Antagonist, Mast Cell Stabilizer
Drug family (ATC)
Antiallergic agents, excl. corticosteroids, Other antiallergics
How it works
Histamine H1 Receptor Antagonists
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.
- RxClass (NLM) · catalog refreshed Oct 1, 2026
Clinical
Label name PATADAY ONCE DAILY 0.2% DROPS Ingredient Olopatadine Hcl
📗 Our plain-language guide HelloPharmacist
- The eye drops relieve itchy eyes from allergies, and some products relieve redness too. The nasal spray relieves seasonal allergic rhinitis symptoms in adults and children 6 and ol...
- It depends on the product. Some eye drops are twice daily, 6 to 8 hours apart, and others once daily. The nasal spray is twice daily. Follow your label or prescriber.
- Take your lenses out before using the drops and wait at least 10 minutes before putting them back. Don't wear lenses if your eyes are red. These drops aren't for contact lens irrit...
- With the nasal spray, a bitter taste, headache, nosebleeds and sore throat are common. It can also make you drowsy, so be careful driving and skip alcohol.
Patient education
Supplement & herbal interactions
Some supplements/herbs that may interact with Olopatadine Hydrochloride — tap one for details:
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 OLOPATADINE HYDROCHLORIDE?
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 mL | 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
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 | Per unit | Per pack | Marketing start | Marketing end | Status |
|---|---|---|---|---|---|---|
| 00065-8150-01 0065-8150-01 Main listing | 1 BOTTLE, PLASTIC in 1 CARTON / 2.5 mL in 1 BOTTLE, PLASTIC | $5.89 / mL | $14.73 | 2020-02-28 | — | Active |
| 00065-8150-03 0065-8150-03 | 2 BOTTLE, PLASTIC in 1 CARTON / 2.5 mL in 1 BOTTLE, PLASTIC | — | — | 2020-02-28 | — | Active |
| 00065-8150-04 0065-8150-04 | 1 BOTTLE, PLASTIC in 1 CARTON / .5 mL in 1 BOTTLE, PLASTIC | — | — | 2020-02-28 | — | Active |
| 00065-8150-07 You're viewing this | 3 BOTTLE, PLASTIC in 1 CARTON / 2.5 mL in 1 BOTTLE, PLASTIC | — | — | 2021-01-15 | — | Active |
This pack shows little to no recent Medicaid volume — a different pack size carries most fills. See all packs ↓
Pack size FAQ
What quantity is in this package?
This package contains 3 bottles — 3 bottle, plastic in 1 carton / 2.5 ml in 1 bottle, plastic.
How does this package differ from NDC 00065-8150-01?
Both are PATADAY ONCE DAILY RELIEF OLOPATADINE HYDROCHLORIDE 2 mg/mL Solution — the drug itself is identical. This page's package is the 3 bottles one, while NDC 00065-8150-01 is the 1 bottle package.
What NDC number is used to bill for this package of PATADAY ONCE DAILY RELIEF OLOPATADINE HYDROCHLORIDE 2 mg/mL Solution?
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.
Prices are the latest CMS NADAC pharmacy acquisition cost per NDC; per-pack figures are per-unit × pack quantity, shown only when the pack is denominated in the same measure NADAC prices.
Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Olopatadine Hydrochloride 2 mg/mL 24208-0617-01 | Bausch | 1 bottle | $1.983 | — | Availability likely | — |
| Leader Olopatadine Hydrochloride 2 mg/mL 70000-0716-01 | CARDINAL | 1 bottle | $1.983 | — | Availability likely | — |
| Olopatadine Hydrochloride 2 mg/mL 00536-1307-23 | Rugby | 1 bottle | $2.964 | — | Availability likely | — |
| olopatadine hydrochloride 2 mg/mL 16571-0861-25 | Rising | 2.5 ml | $2.964 | — | Availability likely | — |
| Olopatadine Hydrochloride Ophthalmic Solution 2 mg/mL 43598-0764-02 | Dr. | 1 bottle | $2.964 | — | Availability likely | — |
| Olopatadine Hydrochloride 2 mg/mL 46122-0671-27 | Amerisource | 1 bottle | $2.964 | — | Availability likely | — |
| Olopatadine Hydrochloride 2 mg/mL 68001-0530-69 | BluePoint | 1 bottle | $2.964 | — | Availability likely | — |
| Olopatadine Hydrochloride 2 mg/mL 68001-0674-92 | BluePoint | 1 bottle | $2.964 | — | Availability likely | — |
| Olopatadine Hydrochloride 2 mg/mL 70069-0491-01 | Somerset | 1 bottle | $2.964 | — | Availability likely | — |
| Eye Allergy Itch Relief Once Daily Relief 2 mg/mL 70677-1155-01 | Strategic | 1 bottle | $2.964 | — | Availability likely | — |
| Olopatadine Hydrochloride Ophthalmic Solution 2 mg/mL 83324-0120-25 | Chain | 1 bottle | $2.964 | — | Availability likely | — |
| Eye Allergy Itch Relief 2 mg/mL 70000-0053-01 | CARDINAL | 1 bottle | $3.096 | — | Availability likely | — |
| Pataday Once Daily Relief 2 mg/mLthis 00065-8150-07 | Alcon | 3 bottles | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 00363-0869-01 | WALGREEN | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride Ophthalmic Solution 2 mg/mL 00363-7131-25 | Walgreens | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 00363-8022-39 | WALGREEN | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride Ophthalmic Solution 2 mg/mL 11673-0688-25 | Target | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 11822-0063-02 | RITE | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride Ophthalmic Solution 2 mg/mL 11822-9975-02 | Rite | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride Ophthalmic Solution 2 mg/mL 21130-0105-02 | Albertsons | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 24208-0967-01 | Bausch | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 30142-0026-27 | Kroger | 1 bottle | — | — | FDA listed | — |
| Once Daily Relief 2 mg/mL 37808-0045-25 | H | 1 bottle | — | — | FDA listed | — |
| Eye Allergy Itch Relief Once Daily Relief 2 mg/mL 43598-0827-02 | Dr. | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 46122-0824-29 | AmerisourceBergen | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 46708-0710-03 | Alembic | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 50090-5613-00 | A-S | 1 bottle | — | — | FDA listed | — |
| Allergy Relief Eye Drops 2 mg/mL 51316-0675-25 | CVS | 1 bottle | — | — | FDA listed | — |
| Retaine Allergy 5 mg/2.5mL 54799-0920-25 | OCuSOFT | 2.5 ml | — | — | FDA listed | — |
| Olopatadine Hydrochloride Ophthalmic Solution Once Daily 2 mg/mL 55910-0137-25 | DOLGENCORP, | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 58602-0007-39 | Aurohealth | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 58602-0010-39 | Aurohealth | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 58602-0013-39 | Aurohealth | 1 bottle | — | — | FDA listed | — |
| Olopatadine hydrochloride 2 mg/mL 60505-6222-02 | Apotex | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 62332-0502-03 | Alembic | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 62332-0710-03 | Alembic | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride Ophthalmic Solution 2 mg/mL 63868-0821-25 | Chain | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 63941-0024-39 | Best | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride Ophthalmic 2 mg/mL 68083-0231-01 | Gland | 1 bottle | — | — | FDA listed | — |
| Eye Allergy Itch Relief 2 mg/mL 69168-0495-77 | Allegiant | 2 bottles | — | — | FDA listed | — |
| CVS Eye Allergy Itch Relief Once Daily 2 mg/mL 69842-0269-25 | CVS | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 72036-0009-39 | Harris | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 72476-0851-21 | Retail | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 72657-0194-11 | GLENMARK | 2 bottles | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 73581-0709-02 | YYBA | 2 bottles | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 76162-0044-39 | TOPCO | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 79481-1001-02 | Meijer | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 79903-0001-39 | Wal-Mart | 1 bottle | — | — | FDA listed | — |
| Equate Olopatadine Hydrochloride 2 mg/mL 79903-0318-01 | WAL-MART | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 80539-0001-39 | Allwell | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride Ophthalmic Solution 2 mg/mL 82442-0967-02 | TARGET | 1 bottle | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 73581-0712-02 | YYBA | 2 bottles | — | — | FDA listed | — |
| Olopatadine Hydrochloride 2 mg/mL 73581-0713-02 | YYBA | 2 bottles | — | — | FDA listed | — |
About this product: this is the brand-name version. FDA-approved generic versions are listed, and recent pricing/market data suggests they may be 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
🏛️
2020
On the market since
Feb 2020
📍
2026
Currently FDA-listed
6 years listed
🔓
·
Generic versions listed
see equivalents
✅Generic appears available
FDA-approved generic versions are listed, and recent pricing/market data suggests they may be available — see Therapeutic equivalents.
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.
💡 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 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 QTT17582CB
A strong acid used to adjust and maintain the proper pH level in liquid medicines, ensuring stability and preventing breakdown of active ingredients.
-
UNII FZ989GH94E
Povidone is a synthetic polymer made from a plastic-like material. It acts as a binder to hold tablet ingredients together and as a disintegrant to help the tablet break apart in your stomach so the medicine can be absorbed.
-
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 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 GR686LBA74
Sodium phosphate, dibasic is a salt derived from phosphoric acid. It acts as a buffer to help maintain the medicine's pH balance and may serve as a binder or filler in tablets and capsules.
-
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.
8 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesbenzalkonium chloride 0.01%, dibasic sodium phosphate, edetate disodium, hydrochloric acid/sodium hydroxide (adjust pH), povidone, purified water, 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.- 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
LabelerAlcon Laboratories, Inc.
Application holderALCON LABORATORIES INC
FDA applicationNDA021545 (NDA)
Labeler code00065
First marketedFeb 2020
Product typeHuman Otc Drug
Portfolio55 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
📦 Storage and Handling
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
📄 Do Not Use
📄 Stop Use and Ask a Doctor If
📄 Keep Out of Reach of Children
📄 Questions or Comments
📄 Package Label / Principal Display Panel
🎯 Indications and Usage ▾
Use temporarily relieves itchy eyes due to pollen, ragweed, grass, animal hair and dander
⏱️ Dosage and Administration ▾
Directions adults and children 2 years of age and older: put 1 drop in the affected eye(s) once daily, no more than once per day if using other ophthalmic products while using this product, wait at least 5 minutes between each product replace cap after each use children under 2 years of age: consult a doctor
⚠️ Warnings ▾
Warnings For external use only
📦 Storage and Handling ▾
Other information only for use in the eye store between 2°-25°C (36°-77°F)
🧪 Active Ingredient ▾
Active Ingredients Purpose Olopatadine 0.2% (equivalent to olopatadine hydrochloride 0.222%) Antihistamine
🧪 Inactive Ingredients ▾
Inactive ingredients benzalkonium chloride 0.01%, dibasic sodium phosphate, edetate disodium, hydrochloric acid/sodium hydroxide (adjust pH), povidone, purified water, and sodium chloride
🎯 Purpose ▾
Active Ingredients Purpose Olopatadine 0.2% (equivalent to olopatadine hydrochloride 0.222%) Antihistamine
📄 Do Not Use ▾
Do not use if solution changes color or becomes cloudy if you are sensitive to any ingredient in this product to treat contact lens related irritation
When using this product do not touch tip of container to any surface to avoid contamination remove contact lenses before use wait at least 10 minutes before reinserting contact lenses after use do not wear a contact lens if your eye is red
📄 Stop Use and Ask a Doctor If ▾
Stop use and ask a doctor if you experience: eye pain changes in vision increased redness of the eye itching worsens or lasts 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.
📄 Questions or Comments ▾
Questions? In the U.S., call 1-800-757-9195 or email [email protected]
📄 Package Label / Principal Display Panel ▾
PRINCIPAL DISPLAY PANEL Pataday ® ONCE DAILY RELIEF Olopatadine hydrochloride ophthalmic solution 0.2% Antihistamine 2.5 mL (0.085 FL OZ) STERILE EYE ALLERGY ITCH RELIEF Only for use in the eye. Store between 2°– 25° C (36°– 77° F) TAMPER EVIDENT: For your protection, this bottle has a seal imprinted with Alcon around the neck. Do not use if seal is damaged or missing at time of purchase.
Alcon Laboratories, Inc. Fort Worth, TX 76134 LOT: EXP.: H15725-219 Original Prescription Strength Pataday ONCE DAILY RELIEF Olopatadine hydrochloride ophthalmic solution 0.2% Antihistamine Eye Allergy Itch Relief ONCE DAILY Works in Minutes Relief from Allergens: Pet Dander Pollen Grass Ragweed STERILE 2.5 mL (0.085 FL OZ) Alcon Pataday ONCE DAILY RELIEF Eye Allergy Itch Relief Works in Minutes TAMPER EVIDENT: For your protection, this bottle has a seal imprinted with Alcon around the neck. Do not use if seal is damaged or missing at time of purchase.
For Ages 2 and Older 30 DAY SUPPLY ________Fill Line________ Alcon Laboratories, Inc. 6201 South Freeway Fort Worth, Texas 76134 Country of Origin: Japan ACTUAL SIZE NDC: 0065-6150-01 300037159-0520 Pataday ® ONCE DAILY RELIEF Olopatadine hydrochloride ophthalmic solution 0.2% Antihistamine 2.5 mL (0.085 fl oz) STERILE EYE ALLERGY ITCH RELIEF Only for use in the eye. Store between 2°– 25° C (36°– 77° F) TAMPER EVIDENT: For your protection, this bottle has a seal imprinted around the neck.
Do not use if seal is damaged or missing at time of purchase. Alcon Laboratories, Inc. Fort Worth, TX 76134 LOT: EXP.: 300071825 -0425 Original Prescription Strength Pataday ® ONCE DAILY RELIEF Olopatadine hydrochloride ophthalmic solution 0.2% Antihistamine Eye Allergy Itch Relief ONCE DAILY #1 DOCTOR RECOMMENDED OTC EYE ALLERGY BRAND* Works in Minutes Alcon STERILE 2.5 mL (0.085 fl oz) LOT: EXP: Pataday ® ONCE DAILY RELIEF Olopatadine hydrochloride ophthalmic solution 0.7% Antihistamine Eye Allergy Itch Relief Pataday ® ONCE DAILY RELIEF Eye Allergy Itch Relief Works in minutes TAMPER EVIDENT: For your protection, this bottle has a seal imprinted around the neck.
Do not use if seal is damaged or missing at time of purchase. For Ages 2 and older 30 DAY SUPPLY ________Fill Line________ Alcon Laboratories, Inc. 6201 South Freeway Fort Worth, Texas 76134 Country of Origin: Japan ACTUAL SIZE NDC: 0065-8150-01 300071461-0325 *Based on a survey of eye care professionals, allergist, and primary care doctors.
December 2024.
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 ↗
Medicaid utilization by pack size
Medicaid (SDUD) totals over the four most recent reported quarters for every package size of this drug — handy when a specific package (e.g. a starter/titration pack) carries little or no Medicaid volume on its own.
Drug total (last 4 qtrs): 19,245 Rx · 55,296 units · $559,209 gross reimbursed
Tap a pack size to open its page. Source: CMS State Drug Utilization Data, last 4 quarters.
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 PATADAY ONCE DAILY RELIEF (this brand).
Top reported reactions
Age at onset
Reporter sex
Male · 31%
Female · 69%
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
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
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 Alcon Laboratories, 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 3 other package presentations of this same product, including 1 bottle (00065-8150-01), 1 bottle (00065-8150-04), 2 bottles (00065-8150-03). 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?
Alcon Laboratories, 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.