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Kinfield Relief Balm Anti-Itch Remedy 10 g/17g Lotion — NDC 81750-0020-40 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Kinfield Relief Balm Anti-Itch Remedy 10 g/17g Lotion — NDC 81750-020-40 (Billing 81750-0020-40)

by Kinfield, Inc. · 1 TUBE in 1 PACKAGE / 40 g in 1 TUBE

This is a package of Kinfield Relief Balm Anti-Itch Remedy 10 g/17g Lotion from Kinfield, Inc., marketed since Apr 2021 and currently FDA-listed.

NDC 81750-0020-40
🏷️ FDA NDC (as labeled) 81750-020-40 billing pads the product segment with a zero
This package
Contains40 g in 1 tube Pack sizes2 compare ↓
Product page 81750-0020-17 Also comes in: 17 g 81750-020-17
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 81750-020-40 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
81750 labeler · 020 product · 40 package
Package marketed since
Apr 5, 2021
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 8175002040 2
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 81750-020-40
Product NDC 81750-020
11-digit billing NDC 81750002040
UNII 8PI54V663Y
Application # M016
SPL Set ID bf394192-c789-faff-e053-2995a90a52bc
Established class (EPC) Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract
Physiologic effect Increased Histamine Release; Cell-mediated Immunity
Chemical class Allergens; Dietary Proteins; Plant Proteins
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-04-05
Route TOPICAL
Dosage form LOTION
Substance OATMEAL
Why two NDCs? The FDA registers this code as 81750-020-40 — 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 → 81750-0020-40. 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?

Kinfield Relief Balm is an over-the-counter lotion applied to the skin to help calm itching and irritation. The product contains oatmeal as its active ingredient, which is commonly used in topical remedies for its soothing properties on irritated skin. This is an OTC monograph drug, meaning it is marketed under FDA's established rules for this category of skin-care products rather than as an individually approved application.

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: 17 g
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
81750-0020-17 81750-020-17 Main listing 1 TUBE in 1 PACKAGE / 17 g in 1 TUBE 2021-04-05 — Active
81750-0020-40 You're viewing this 1 TUBE in 1 PACKAGE / 40 g in 1 TUBE 2021-04-05 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 tube in 1 package / 40 g in 1 tube.
What NDC number is used to bill for this package of Kinfield Relief Balm Anti-Itch Remedy 10 g/17g Lotion?
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
Kinfield Relief Balm Anti-Itch Remedy 10 g/17gthis 81750-0020-40 Kinfield, 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

🏛️
2021
On the market since
Apr 2021
📍
2026
Currently FDA-listed
5 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 9E8X80D2L0
    A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
  • UNII LP618AV2EA
    A natural oil derived from chamomile and other plants. It serves as a fragrance and flavoring agent to improve the taste and smell of the medicine.
  • UNII OZ0E5Y15PZ
    A plant extract from arnica flowers, used as a flavoring agent or fragrance component in medicines. It may also provide mild soothing properties to certain topical formulations.
  • UNII WL0328HX19
    A natural plant-based wax derived from candelilla shrub leaves. It acts as a coating agent, hardener, and texture modifier to control how quickly the medicine releases and to improve the tablet or capsule's appearance and stability.
  • UNII 245J88W96L
    A plant-derived ingredient from coconut that acts as a filler and texture agent in medications. It helps create the proper consistency and bulk needed for tablets or capsules.
  • UNII W5488JUO8U
    A plant extract from turmeric root used as a natural colorant and flavoring agent in medicines. It provides yellow-to-orange color and mild spice flavor to tablets, capsules, and liquids.
  • UNII XE7K568ILO
    A plant-derived oil from lemongrass used as a flavoring agent and fragrance component. It adds taste and aroma to medicines, making them more palatable.
  • UNII UEG2DV5C8N
    A plant-derived oil from the African oil palm used as a lubricant and binder in tablet and capsule formulations to improve manufacturing flow and reduce sticking.
  • UNII S546YLW6E6
    Eucalyptus globulus leaf is a plant-derived ingredient that may serve as a flavoring agent or aromatic component in medications. It is commonly used to add taste or scent to oral formulations.
  • UNII 17S27ZT6KR
    A plant extract from sunflower seeds used as a natural emulsifier and skin-conditioning agent in topical formulations. It helps blend oil and water components together and softens the product texture.
  • UNII K62C66D9LN
    A plant extract from cajeput tree leaves, used as a fragrance, flavoring, or preservative in medicines to improve taste, smell, or shelf stability.
  • UNII L7T10EIP3A
    A cooling compound from mint plants used as a flavoring agent and to create a fresh sensation in medicines. It helps mask bitter tastes and improve how the product feels in the mouth.
  • UNII LAV5U5022Y
    Methyl salicylate is a naturally derived liquid compound commonly found in wintergreen plants. In medicines, it's used as a flavoring agent and penetrating solvent to help distribute active ingredients evenly throughout topical products.
  • UNII 8490RQ2BET
    A plant extract from avocado leaves used as a natural flavoring agent or preservative in medicines. It may help preserve the product or add subtle flavor.
  • UNII K49155WL9Y
    Shea butter is a fat extracted from shea tree nuts. It's used in medicines as an emollient and lubricant to soften the product, improve texture, and help ingredients blend smoothly together.
  • UNII DFM16KFA82
    A plant oil extracted from jojoba seeds, used as an emollient and conditioning agent. It helps soften the formulation and improve how the medicine feels on skin or in the mouth.

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

The official label also statesCocos Nucifera Oil, Euphorbia Cerifera Wax, Caprylic/Capric Triglyceride, Melaleuca Cajuputi Oil, Eucalyptus Globulus Leaf Oil, Tocopheryl Acetate, Menthol, Methyl Salicylate, Butyrospermum Parkii Butter, Helianthus Annuus Seed Oil, Persea Gratissima Oil, Cymbopogon Schoenanthus Oil, Arnica Montana Flower Extract, Elaeis Guineensis Butter, Simmondsia Chinensis Seed Oil, Curcuma Longa Root Extract, Bisabolol

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

LabelerKinfield, Inc.
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code81750
First marketedApr 2021
Product typeHuman Otc Drug
Portfolio6 products on file

More NDCs from Kinfield, Inc. labeler code 81750

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 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 15 words ▾

Uses Temporarily protects and helps releive minor skin irritation and itching due to insect bites

⏱️ Dosage and Administration 4 words ▾

Directions Apply as needed.

⚠️ Warnings 39 words ▾

Warnings Fox external use only. 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

🧪 Active Ingredient 5 words ▾

Active Ingredients Colloidal Oatmeal 10.00%

🧪 Inactive Ingredients 51 words ▾

Inactive Ingredients Cocos Nucifera Oil, Euphorbia Cerifera Wax, Caprylic/Capric Triglyceride, Melaleuca Cajuputi Oil, Eucalyptus Globulus Leaf Oil, Tocopheryl Acetate, Menthol, Methyl Salicylate, Butyrospermum Parkii Butter, Helianthus Annuus Seed Oil, Persea Gratissima Oil, Cymbopogon Schoenanthus Oil, Arnica Montana Flower Extract, Elaeis Guineensis Butter, Simmondsia Chinensis Seed Oil, Curcuma Longa Root Extract, Bisabolol

🎯 Purpose 3 words ▾

Purpose Skin Protectant

📄 Keep Out of Reach of Children 38 words ▾

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

📄 Package Label / Principal Display Panel 4 words ▾

Principal Display Panel 81750-020-17

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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 Kinfield, 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 1 other package presentation of this same product, including 1 tube (81750-0020-17). 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?
Kinfield, 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.
← 81750-0010-60 · Kinfield, 81750-0041-03 · Kinfield, →
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.