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Lice-Nil LICE AND EGGS ELIMINATOR Oil AZADIRACHTA INDICA 1 [hp_X]/100mL Oil — NDC 76441-0909-94 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Lice-Nil LICE AND EGGS ELIMINATOR Oil AZADIRACHTA INDICA 1 [hp_X]/100mL Oil — NDC 76441-909-94 (Billing 76441-0909-94)

by Sujanil Chemo Industries · 1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE

This is a package of Lice-Nil LICE AND EGGS ELIMINATOR Oil AZADIRACHTA INDICA 1 [hp_X]/100mL Oil from Sujanil Chemo Industries, marketed since Aug 2017 and currently FDA-listed. It is this product's only package size.

NDC 76441-0909-94
🏷️ FDA NDC (as labeled) 76441-909-94 billing pads the product segment with a zero
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 76441-909-94 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
76441 labeler · 909 product · 94 package
Package marketed since
Aug 1, 2017
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0863234000402
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 76441-909-94
Product NDC 76441-909
11-digit billing NDC 76441090994
UNII 4DKJ9B3K2T
UPC 0863234000402
SPL Set ID 39dea217-157e-4cd4-b153-6b2f9227ea78
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2017-08-01
Route TOPICAL
Dosage form OIL
Substance AZADIRACHTA INDICA SEED OIL
Why two NDCs? The FDA registers this code as 76441-909-94 — 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 → 76441-0909-94. 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

🧪 What is this product?

Lice-Nil Lice and Eggs Eliminator is a topical oil containing azadirachta indica (neem) seed oil marketed as a homeopathic product. In homeopathic practice, neem oil is traditionally used for head lice and nit removal. This product is not evaluated by the FDA for effectiveness and is marketed based on homeopathic tradition rather than clinical evidence. It is applied directly to the scalp and hair as an unapproved homeopathic remedy.

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 eachPer 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
76441-0909-94 You're viewing this Main listing 1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE 2017-08-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Lice-Nil LICE AND EGGS ELIMINATOR Oil 1 [hp_X]/100mLthis 76441-0909-94 Sujanil 1 bottle — — 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

🏛️
2017
On the market since
Aug 2017
📍
2026
Currently FDA-listed
9 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 H4N855PNZ1
    Alpha-tocopherol is a form of vitamin E, a fat-soluble antioxidant derived from natural or synthetic sources. In medicines, it prevents oils and fats from breaking down and becoming rancid, protecting the product's stability and shelf life.
  • UNII Q9L0O73W7L
    Coconut oil is a natural fat extracted from coconut fruit. It's used in medicines as a lubricant, emollient, or carrier to help dissolve or deliver active ingredients smoothly through the formulation.
  • UNII PAD4FN7P2G
    A fragrant essential oil from juniper wood, used primarily as a flavoring agent and fragrance component to mask tastes and add aroma to medicines.
  • UNII ZBP1YXW0H8
    A fragrant oil extracted from lavender plants, used as a flavoring and scent agent in medicines to improve taste and aroma.
  • UNII I9GRO824LL
    Lemon oil is a natural fragrant extract from lemon peel. It's used in medicines as a flavoring agent to mask unpleasant tastes and improve how the medicine tastes to patients.
  • UNII 8LGU7VM393
    Rosemary leaf oil is a natural aromatic oil extracted from rosemary plants. It's used in medicines as a flavoring agent and preservative to help protect the product from spoilage.
  • UNII QX10HYY4QV
    Sesame oil is a plant-derived oil from sesame seeds. It's used in medicines as a solvent or carrier to dissolve or suspend active ingredients, helping them mix evenly throughout the formulation.
  • UNII 3W1JG795YI
    Sunflower oil is a natural vegetable oil derived from sunflower seeds. It serves as a solvent, lubricant, and carrier in medicines, helping dissolve active ingredients and improve how the medication flows and absorbs in the body.
  • UNII VIF565UC2G
    Tea tree oil is an essential oil extracted from the leaves of the Australian tea tree plant. In medicines, it typically serves as a flavoring agent, fragrance, or antimicrobial component in topical formulations.

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

The official label also statesCoconut Oil, Sesame Oil, Tea Tree Oil, Sunflower Oil with Herbal Extracts and Perfumes

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

LabelerSujanil Chemo Industries
Labeler code76441
First marketedAug 2017
Product typeHuman Otc Drug
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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 10 words ▾

Uses: Treats head lice/nits, pubic lice (crab) and body lice

⏱️ Dosage and Administration ~1 min read ▾

Directions Inspect Check each household member with a magnifying glass in bright light for lice/nits (eggs) Look for tiny nits near scalp, beginning at back of neck and behind ears Examine small sections of hair at a time Unlike dandruff which moves when touched, nits stick to the roots of hair If either lice or nits are found, treat with this product Treat Apply thoroughly to dry hair or other affected area. For head lice, first apply on hair behind ears and back of neck, then continue to apply to the remainder of hair Leave product on hair for a minimum of 20 minutes Wash area thoroughly with warm water and shampoo or soap after treatment For head lice, towel dry hair and comb out tangles Remove lice and their eggs (nits) Using a fine-tooth comb or special lice/nit comb, remove any remaining nits by hand.

For head lice, part hair into sections and inspect one section at a time, starting at the top of head. Longer hair may take 1-2 hours. Lift a 1-2-inch wide strand of hair.

Place comb with a firm, even motion away from scalp. Pin back each strand of hair after combing Clean comb often. Wipe nits away with tissue and discard in a plastic bag.

Seal bag and discard to prevent lice from coming back After combing, thoroughly recheck for lice/nits. Repeat combing if necessary Check daily for any lice/nits that may have been missed We recommend a second treatment after 7-10 days to kill any newly hatched lice Children under 2 years: Consult with a Doctor or Physician

⚠️ Warnings 84 words ▾

Warnings For External Use Only Do not use: Near eyes Inside nose, mouth or vagina On lice in eyebrows or eyelashes. See a doctor if lice are present in these areas Ask a Doctor before use if you are: Allergic to ragweed. May cause breathing difficulty or an asthmatic attack When using this product: If product gets in eyes, flush with water right away Stop use and ask a doctor if: Breathing difficulty occurs Eye irritation occurs Skin or scalp irritation or infection occurs

📦 Storage and Handling 24 words ▾

Other information Shake well before use Store in cool and dry place Keep carton for important product information See package insert for additional information

🧪 Active Ingredient 6 words ▾

Active Ingredients Azadirachta Indica (NEEM) 1X

🧪 Inactive Ingredients 16 words ▾

Inactive ingredients: Coconut Oil, Sesame Oil, Tea Tree Oil, Sunflower Oil with Herbal Extracts and Perfumes

🎯 Purpose 3 words ▾

Purpose Lice treatment.

📄 Keep Out of Reach of Children 32 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away Important: Read warnings before use For Adults and Children 2 years and older

📄 Questions or Comments 10 words ▾

Questions or comments? 855-KIL-LICE - 855-545-5423 www.licenil.com or e-mail: [email protected]

📄 Package Label / Principal Display Panel 3 words ▾

Packaging image description

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 Lice-Nil LICE AND EGGS ELIMINATOR Oil (this brand).

Top reported reactions

Hyponatraemia7

Reporter sex

7 reports
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 Homeopathic listing

About homeopathic listings

Lice-Nil LICE AND EGGS ELIMINATOR Oil AZADIRACHTA INDICA 1 [hp_X]/100mL OIL is listed under the homeopathic marketing category. An NDC listing in this category does not by itself establish FDA approval, and FDA does not evaluate homeopathic products for effectiveness. This page reports the listing data as published.

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 "Unapproved Homeopathic". 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 Sujanil Chemo Industries. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Sujanil Chemo Industries 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.
← 76438-0007-00 · Anthem 76446-0022-50 · Anna →
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.