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Leader Nighttime Relief Lubricant Eye Light Mineral Oil, White Petrolatum 425 mg/g; 573 mg/g Ointment, 1 tube — NDC 70000-0724-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Leader Nighttime Relief Lubricant Eye Light Mineral Oil, White Petrolatum 425 mg/g; 573 mg/g Ointment, 1 tube — NDC 70000-0724-1 (Billing 70000-0724-01)

by LEADER/Cardinal Health 110, Inc. · 1 TUBE in 1 BOX / 3.5 g in 1 TUBE

This is a package of 1 tube of Leader Nighttime Relief Lubricant Eye Light Mineral Oil, White Petrolatum 425 mg/g; 573 mg/g Ointment from LEADER/Cardinal Health 110, Inc., marketed since Mar 2025 and currently FDA-listed; retail pharmacies pay about $1.49 per g (NADAC). It is this product's only package size.

NDC 70000-0724-01
🏷️ FDA NDC (as labeled) 70000-0724-1 billing pads the package segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

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

NDC database record

One package, one record: these facts belong to NDC 70000-0724-1 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
70000 labeler · 0724 product · 1 package
Package marketed since
Mar 12, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0096295145014
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 70000-0724-1
Product NDC 70000-0724
11-digit billing NDC 70000072401
NCPDP billing unit GM — per gram (weight)
RxCUI 702008
UNII N6K5787QVP, B6E5W8RQJ4
UPC 0096295145014
Application # M018
SPL Set ID 308772fc-d6f6-da9f-e063-6394a90a41db
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-03-12
Route OPHTHALMIC
Dosage form OINTMENT
Substance LIGHT MINERAL OIL; WHITE PETROLATUM

Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification

GPI-14 86209902904220
GCN Seq No 065933
GCN 28068
HICL code 002215
Ingredient (HICL) Mineral Oil/Petrolatum,White
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 Q6Y
Therapeutic class — specific (HIC3) Eye Preparations, Miscellaneous (Otc)
AHFS code 52:92.00.00
AHFS class Eent Drugs, Miscellaneous
FDB label name NIGHTTIME LUBRICANT EYE OINT
FDB brand name Nighttime Relief Lubricant Eye
Legend status O — Over-the-counter (OTC) drug or device
Quick answers
  • GSN (GCN sequence number): 065933
  • GCN: 28068
  • GPI-14 (Medi-Span): 86209902904220
  • HICL (First Databank): 002215
  • AHFS class code: 52:92.00.00
  • RxCUI (RxNorm): 702008
Why two NDCs? The FDA registers this code as 70000-0724-1 — 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 → 70000-0724-01. 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 Softeners, emollients class.

Drug family (ATC) Softeners, emollients
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

Label name NIGHTTIME LUBRICANT EYE OINT Ingredient Mineral Oil/Petrolatum,White
🧪 What is this product?

Leader Nighttime Relief Lubricant Eye is an over-the-counter ointment applied directly to the eye. It contains light mineral oil and white petrolatum, which are occlusive lubricants typically used to coat and protect the eye surface. This type of product is commonly used at bedtime to soothe dry eyes and create a protective barrier that slows tear evaporation overnight.

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 gPer package
Retail pharmacies payNADAC · weekly $1.488 $5.21 / 3.5 g
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.
NADAC price history (per g) — tap or hover for the price & month
May 2026 Jun 2026 Jul 2026 Sep 2026 $1.702 $1.447
▼ Down 13% over the last 5 months.
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
70000-0724-01 You're viewing this Main listing 1 TUBE in 1 BOX / 3.5 g in 1 TUBE 2025-03-12 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Nighttime Relief Lubricant 425 mg/g; 573 mg/g 46122-0757-37 Amerisource 1 tube $1.488 — Availability likely —
Leader Nighttime Relief Lubricant Eye 425 mg/g; 573 mg/gthis 70000-0724-01 LEADER/Cardinal 1 tube $1.488 — Availability likely —
Refresh P.m. 425 mg/g; 573 mg/g 00023-0667-04 Allergan, 1 tube $2.449 — Availability likely +65%
Equate Nighttime Relief Lubricant 425 mg/g; 573 mg/g 11716-0367-01 Hanlim 1 tube — — FDA listed —
Lubricant Eye PM 42.5 g/100g; 57.3 g/100g 69618-0060-76 Reliable 1 tube — — FDA listed —
Equate Nighttime Relief Lubricant 425 mg/g; 573 mg/g 79903-0260-35 Walmart 1 tube — — FDA listed —
Equate Nighttime Relief Lubricant 425 mg/g; 573 mg/g 79903-0367-01 Walmart 1 tube — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2025
On the market since
Mar 2025
📍
2026
Currently FDA-listed
1 year listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 884C3FA9HE
    Lanolin alcohol is a waxy substance derived from sheep's wool. It functions as an emollient and emulsifier in medicines, helping blend oil and water-based ingredients while softening the product's texture.

1 inactive ingredient listed in the exact product block matched to this NDC.

The official label also stateslanolin alcohols

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

LabelerLEADER/Cardinal Health 110, Inc.
FDA applicationM018 (OTC MONOGRAPH DRUG)
Labeler code70000
First marketedMar 2025
Product typeHuman Otc Drug
Portfolio4 products on file

More NDCs from LEADER/Cardinal Health 110, Inc. labeler code 70000

The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 31 words ▾

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 23 words ▾

Directions pull down the lower lid of the affected eye apply a small amount (1/4 inch) of ointment to the inside of eyelid

⚠️ Warnings 92 words ▾

Warnings For external use only Do not use except under the advice and supervision of a doctor When using this product replace cap after use to avoid contamination do not touch tip of container to any surface remove contact lenses before using Stop use and ask a doctor if you experience eye pain, changes in vision, continued redness or irritation of the eye 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 (1-800-222-1222) right away.

🧪 Active Ingredient 9 words ▾

Active ingredients Light Mineral Oil 42.5% White Petrolatum 57.3%

🧪 Inactive Ingredients 4 words ▾

Inactive ingredient lanolin alcohols

🎯 Purpose 5 words ▾

Purposes Eye Lubricant Eye Lubricant

📄 Do Not Use 12 words ▾

Do not use except under the advice and supervision of a doctor

📄 When Using This Product 25 words ▾

When using this product replace cap after use to avoid contamination do not touch tip of container to any surface remove contact lenses before using

📄 Stop Use and Ask a Doctor If 30 words ▾

Stop use and ask a doctor if you experience eye pain, changes in vision, continued redness or irritation of the eye condition worsens or persists for more than 72 hours

📄 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 (1-800-222-1222) right away.

📄 Other Information 41 words ▾

Other information store at 15-25ºC (59-77°F) DO NOT FREEZE keep tightly closed do not use if difficult to dispense or visible particles are seen in the product do not roll, bend, twist, or fold tube during use store away from heat

📄 Questions or Comments 5 words ▾

Questions or comments? Call 1-888-527-4276

📄 Package Label / Principal Display Panel 13 words ▾

Leader Nighttime Relief Lubricant Eye Ointment 3.5g Leader Nighttime Relief Lubricant Eye Ointment

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 70000-0723-01 · Cardinal 70000-0725-01 · Cardinal →
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.