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Lanashield Lanolin 50 g/100g Ointment — NDC 67777-0410-07 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Lanashield Lanolin 50 g/100g Ointment — NDC 67777-410-07 (Billing 67777-0410-07)

by Dynarex Corporation · 2 BOX in 1 CASE / 144 PACKET in 1 BOX / 5 g in 1 PACKET

This is a package of Lanashield Lanolin 50 g/100g Ointment from Dynarex Corporation, marketed since Oct 2014 and currently FDA-listed.

NDC 67777-0410-07
🏷️ FDA NDC (as labeled) 67777-410-07 billing pads the product segment with a zero
This package
Contains5 g in 1 packet Pack sizes4 compare ↓
Product page 67777-0410-03 Also comes in: 12 jars 67777-410-14 24 tubes 67777-410-03 36 jars 67777-410-12
OTC On market Non-controlled ⇄ 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

NDC database record

One package, one record: these facts belong to NDC 67777-410-07 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
67777 labeler · 410 product · 07 package
Package marketed since
Oct 12, 2014
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0616784126319, 0840117346857, 0840117346802, 0840117346826
FDA record last changed
Jul 24, 2026
⚠️
Other active recalls for Lanolin (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Aug 27, 2025 — CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. (DermaRite Industries, LLC) · FDA recall D-0171-2026
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) 67777-410-07
Product NDC 67777-410
11-digit billing NDC 67777041007
RxCUI 853167, 1552270
UNII 7EV65EAW6H
UPC 0616784126319, 0840117346857, 0840117346802, 0840117346826
Application # M016
SPL Set ID 94b277dc-6512-4d36-8485-8ea510097428
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2014-10-12
Route TOPICAL
Dosage form OINTMENT
Substance LANOLIN

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

GPI-14 90972000003700
GCN Seq No 065122
GCN 22542
HICL code 002208
Ingredient (HICL) Lanolin
HIC1 code L
Therapeutic class — broad (HIC1) Skin/Subcutaneous Tissue
HIC2 code L2
Therapeutic class — intermediate (HIC2) Emollients
HIC3 code L2A
Therapeutic class — specific (HIC3) Emollients
AHFS code 84:24.12.00
AHFS class Basic Ointments And Protectants
FDB label name LANASHIELD 50% OINTMENT
FDB brand name Lanashield
Legend status O — Over-the-counter (OTC) drug or device
Quick answers
  • GSN (GCN sequence number): 065122
  • GCN: 22542
  • GPI-14 (Medi-Span): 90972000003700
  • HICL (First Databank): 002208
  • AHFS class code: 84:24.12.00
  • RxCUI (RxNorm): 853167
Why two NDCs? The FDA registers this code as 67777-410-07 — 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 → 67777-0410-07. 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.

Clinical

Label name LANASHIELD 50% OINTMENT Ingredient Lanolin
🧪 What is this product?

Lanashield Lanolin is an over-the-counter topical ointment containing lanolin, a waxy substance derived from sheep's wool. Lanolin is commonly used in skin care products as an emollient and moisturizer to help soften and protect the skin. This product is marketed under the FDA's OTC monograph rules for skin protectant products rather than through individual drug approval.

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 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: 12 jars 24 tubes 36 jars
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
67777-0410-03 67777-410-03 Main listing 24 TUBE in 1 CASE / 113 g in 1 TUBE 2014-10-12 — Active
67777-0410-07 You're viewing this 2 BOX in 1 CASE / 144 PACKET in 1 BOX / 5 g in 1 PACKET 2014-10-12 — Active
67777-0410-12 67777-410-12 36 JAR in 1 CASE / 71 g in 1 JAR 2014-10-12 — Active
67777-0410-14 67777-410-14 12 JAR in 1 CASE / 397 g in 1 JAR 2014-10-12 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 2 box in 1 case / 144 packet in 1 box / 5 g in 1 packet.
What NDC number is used to bill for this package of Lanashield Lanolin 50 g/100g Ointment?
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
Lanashield 50 g/100gthis 67777-0410-07 Dynarex 144 packets — — FDA listed —
Skin Protectant with Lanolin 50 g/100g 68599-6202-04 McKesson 144 packets — — FDA listed —
Skin Protectant with Lanolin 50 g/100g 68599-6203-04 McKesson 24 tubes — — FDA listed —
Lanolin 50% 50 g/100g 87236-0019-04 Aldermed 113 g — — FDA listed —
ClaraVie 50 g/100g 61554-0307-11 Gentell 113 g — — 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

🏛️
2014
On the market since
Oct 2014
📍
2026
Currently FDA-listed
12 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 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 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.
  • UNII T5L8T28FGP
    Mineral oil is a clear, odorless liquid derived from crude oil. It acts as a lubricant and emollient in medications, helping pills slide smoothly during manufacturing and aiding moisture retention in topical products.
  • 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 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.
  • UNII B6E5W8RQJ4
    White petrolatum is a purified mineral oil product used as a lubricant and skin protectant in medications. It helps pills slide through manufacturing equipment and can soften or protect the skin when applied topically.
  • UNII 7G1J5DA97F
    White wax is a refined, bleached plant-based or mineral wax that serves as a coating and hardening agent in medicines. It helps control how fast the drug dissolves and improves the product's texture and appearance.

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

The official label also statesbeeswax (White), edetate disodium, emulsifying wax, lanolin alcohol, mineral oil, mint perfume, petrolatum, purified water, sodium borate

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

LabelerDynarex Corporation
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code67777
First marketedOct 2014
Product typeHuman Otc Drug
Portfolio60 products on file

More NDCs from Dynarex Corporation labeler code 67777

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 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Other Information 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 35 words ▾

Uses Temporarily protects minor • cuts • scrapes • burns Temporarily protects and helps relieve chafed, chapped, or cracked skin and lips Helps prevent and protect from the drying effects of wind and cold weather

⏱️ Dosage and Administration 4 words ▾

Directions Apply as needed

⚠️ Warnings 87 words ▾

Warnings For External Use Only Do not use on • Deep or puncture wounds • Animal bites • Serious burns When using this product • Do not get into eyes. Stop use and ask a doctor if • Condition worsens • Symptoms last more than 7 days or clear up and occur again within a few days 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 (1-800-222-1222) Center right away.

🧪 Active Ingredient 5 words ▾

Active Ingredient Lanolin USP 50%

🧪 Inactive Ingredients 19 words ▾

Inactive Ingredients beeswax (White), edetate disodium, emulsifying wax, lanolin alcohol, mineral oil, mint perfume, petrolatum, purified water, sodium borate

🎯 Purpose 3 words ▾

Purpose Skin Protectant

📄 Do Not Use 15 words ▾

Do not use on • Deep or puncture wounds • Animal bites • Serious burns

📄 When Using This Product 10 words ▾

When using this product • Do not get into eyes.

📄 Stop Use and Ask a Doctor If 27 words ▾

Stop use and ask a doctor if • Condition worsens • Symptoms last more than 7 days or clear up and occur again within a few days

🤰 If Pregnant or Breast-Feeding 10 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 (1-800-222-1222) Center right away.

📄 Other Information 20 words ▾

Other Information Store at room temperature 15º-30ºC (59º-86ºF) Avoid excessive heat Tamper evident. Do not use if seal is damaged.

📄 Package Label / Principal Display Panel 8 words ▾

Label 1260_BX_MASTER

Label 1262_IN_MASTER

Label 1263_IN_MASTER

Label 1265_IN_MASTER

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 Lanashield (this brand).

Top reported reactions

Dyspnoea25
Drug Hypersensitivity24
Pneumonia20
Fall17
Death16
Dizziness15
Cough14

Age at onset

Neonate1
Child1
Adolescent2
Adult14
Elderly6

Reporter sex

145 reports
Male · 41%
Female · 59%

Serious outcomes

Hospitalization68
Death36
Life-threatening11
Disabling6
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 15 0
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

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 Dynarex Corporation. 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 12 jars (67777-0410-14), 24 tubes (67777-0410-03), 36 jars (67777-0410-12). 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?
Dynarex Corporation 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.
← 67777-0408-02 · Dynarex 67777-0418-01 · Dynarex →
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.