Home › NDC Lookup › Ingredients › Anti Itch Cream › 84051-0001-01
Anti-Itch Cream 1 [hp_X]/g; 1 [hp_X]/g; 1 [hp_X]/g; 1 [hp_X]/g; 1 [hp_X]/g; 3 [hp_X]/g; 4 [hp_X]/g Cream, 15 g — NDC 84051-0001-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Anti-Itch Cream 1 [hp_X]/g; 1 [hp_X]/g; 1 [hp_X]/g; 1 [hp_X]/g; 1 [hp_X]/g; 3 [hp_X]/g; 4 [hp_X]/g Cream, 15 g — NDC 84051-001-01 (Billing 84051-0001-01)

by Buzzie LLC · 15 g in 1 BOTTLE, PUMP

This is a package of 15 g of Anti-Itch Cream 1 [hp_X]/g; 1 [hp_X]/g; 1 [hp_X]/g; 1 [hp_X]/g; 1 [hp_X]/g; 3 [hp_X]/g; 4 [hp_X]/g Cream from Buzzie LLC, marketed since Mar 2026 and currently FDA-listed. It is this product's only package size.

NDC 84051-0001-01
🏷️ FDA NDC (as labeled) 84051-001-01 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 Sep 10, 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 84051-001-01
Product NDC 84051-001
11-digit billing NDC 84051000101
UNII TRW2FUF47H, O80TY208ZW, XK4IUX8MNB, C88X29Y479, IHN2NQ5OF9, Z5BEX9K2G1 +1 more
SPL Set ID 596d1aae-c97e-c928-e063-6394a90a77d9
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-03-01
Route TOPICAL
Dosage form CREAM
Substance ALTHAEA OFFICINALIS ROOT; ARNICA MONTANA; HYPERICUM PERFORATUM; LYCOPODIUM CLAVATUM SPORE; URTICA URENS; JUNIPERUS SABINA LEAFY TWIG; DAPHNE MEZEREUM BARK
Why two NDCs? The FDA registers this code as 84051-001-01 — 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 → 84051-0001-01. 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.

Clinical

🧪 What is this product?

This is a topical cream marketed as a homeopathic anti-itch product. It contains seven plant-derived ingredients, including arnica, hypericum, urtica urens, and others, that are used in homeopathic practice for purposes such as soothing skin irritation and itching. Homeopathic products are marketed based on homeopathic tradition rather than FDA evaluation for effectiveness. This product is not approved by the FDA as a conventional drug.

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.
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
84051-0001-01 You're viewing this Main listing 15 g in 1 BOTTLE, PUMP 2026-03-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Anti-Itch Cream 1 [hp_X]/g; 1 [hp_X]/g; 1 [hp_X]/g; 1 [hp_X]/g; 1 [hp_X]/g; 3 [hp_X]/g; 4 [hp_X]/gthis 84051-0001-01 Buzzie 15 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

🏛️
2026
On the market since
Mar 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
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 77MKL7AR5I
    A natural oil extracted from baobab tree seeds. It's used as an emollient and skin-conditioning agent to help soften the product texture and improve how the medicine feels on application.
  • UNII 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • UNII 3XUS85K0RA
    Butylene glycol is a clear liquid derived from petroleum or plants that acts as a humectant, solvent, and preservative booster in medicines. It helps keep formulations stable, dissolve active ingredients, and maintain moisture in topical products.
  • UNII 0A5MM307FC
    A synthetic polymer that absorbs water and forms a thick, gel-like substance. In medicines, it works as a thickener and stabilizer to improve texture and help ingredients stay mixed together in creams, gels, and lotions.
  • UNII OO4K72NZ2X
    A plant-derived powder from quinoa seeds, used as a filler and binding agent to give the tablet or capsule structure and help hold its ingredients together during manufacturing and storage.
  • UNII 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • 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.

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

The official label also statesInactive Ingredients Adansonia Digitata (Baobab) Seed Oil, Aqua/Water, Butylene Glycol & Chenopodium Quinoa Seed, Citric Acid, Cross-linked acrylic acid homopolymer, Ethyl Alcohol, Mentha Piperita Oil, Methyl Glucose Dioleate, Sodium Hydroxide

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

LabelerBuzzie LLC
Labeler code84051
First marketedMar 2026
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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 47 words ▾

Uses For the temporary relief of inflammation, pain, itching, burning and stinging sensation. Indications are based on Homeopathic Materia Medica, not clinical testing. Product efficacy and claims are based on theories of homeopathy that are not supported by scientific evidence and most allopathic medical professionals. uses section

⏱️ Dosage and Administration 72 words ▾

Directions: Adults and children 2 years of age and older, apply a thin layer of cream on clean skin to cover the affected area • For best results, allow cream to be absorbed into the skin: do not rub in • Apply at the onset of symptoms, not more than 6 times daily or every 15 minutes for the first hour • Do not use with other topical remedies or lotions. directions

⚠️ Warnings 88 words ▾

Warning For external use only Do not use on damaged or broken skin Keep out of • eyes • open wounds • mucous membranes Stop use and ask a physician if • condition worsens or persist • rash develops Ask a physician before use if you are taking a prescription drug or have a serious medical condition If pregnant or breastfeeding consult your doctor before use Keep out of the reach of children If swallowed, get medical help or contact a Poison Control Center right away warning section

🧪 Active Ingredient 51 words ▾

All active ingredients are HPUS Althaea Officinalis 1X, Arnica Montana 1X, Hypericum Perforatum 1X, Lycopodium Clavatum 1X, Mezereum 4X, Sabina 3X, Urtica Urens 1X Purpose: Anti-inflammatory, Anti-itching & burning, Analgesic, Relieves itching, burning, stinging *HPUS indicates the active ingredients are in the official Homeopathic Pharmacopoeia of the United States. active ingredients

🧪 Inactive Ingredients 32 words ▾

Inactive Ingredients Adansonia Digitata (Baobab) Seed Oil, Aqua/Water, Butylene Glycol & Chenopodium Quinoa Seed, Citric Acid, Cross-linked acrylic acid homopolymer, Ethyl Alcohol, Mentha Piperita Oil, Methyl Glucose Dioleate, Sodium Hydroxide inactive ingredients

🎯 Purpose 12 words ▾

Purpose Anti-inflammatory, Anti-itching & burning, Analgesic Relieves itching, burning, stinging purpose section

📄 Keep Out of Reach of Children 25 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. keep out of reach of children

📄 Other Information 30 words ▾

Other Information Store in a cool dark place away from children • Avoid direct sunlight • Tamper-evident seal for your protection. Use only if safety seal is intact other information

📄 Questions or Comments 9 words ▾

Questions or Comments? Visit us at Buzzie.com question section

📄 Package Label / Principal Display Panel 28 words ▾

FAMILY FRIENDLY* Buzzie ANTI-ITCH CREAM PLANT-POWERED INGREDIENTS The best places in the world are full of bugs NET WT

0.53 OZ (15GM) *when used as directed front panel

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 Anti-Itch Cream — the ingredient across all brands.

Top reported reactions

Fatigue5,917
Condition Aggravated5,454
Nausea4,999
Rash4,909
Diarrhoea4,452
Headache4,425
Pain4,424

Age at onset

Neonate332
Infant314
Child1,040
Adolescent683
Adult7,948
Elderly3,425

Reporter sex

66,661 reports
Male · 42%
Female · 58%
Unknown · 0%

Serious outcomes

Hospitalization28,430
Life-threatening8,647
Reports over time (by year) — tap or hover for the count & year
2021 2022 2024 2026 6,429 2,806
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 Homeopathic listing

About homeopathic listings

Anti-Itch Cream 1 [hp_X]/g; 1 [hp_X]/g; 1 [hp_X]/g; 1 [hp_X]/g; 1 [hp_X]/g; 3 [hp_X]/g; 4 [hp_X]/g CREAM 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 Buzzie LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Buzzie LLC 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.
← 84047-2090-02 · Refy 84053-0025-07 · Martek →
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.