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Eczema Itch Relief Wash and Shampo Colloidal Oatmeal 15 mg/mL Shampoo, 355 mL — NDC 10738-0162-23 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Eczema Itch Relief Wash and Shampo Colloidal Oatmeal 15 mg/mL Shampoo, 355 mL — NDC 10738-162-23 (Billing 10738-0162-23)

by Genuine Virgin Aloe Corporation · 355 mL in 1 BOTTLE

This is a package of 355 mL of Eczema Itch Relief Wash and Shampo Colloidal Oatmeal 15 mg/mL Shampoo from Genuine Virgin Aloe Corporation, marketed since Sep 2020 and currently FDA-listed. It is this product's only package size.

NDC 10738-0162-23
🏷️ FDA NDC (as labeled) 10738-162-23 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 10738-162-23
Product NDC 10738-162
11-digit billing NDC 10738016223
RxCUI 2396990
UNII 8PI54V663Y
UPC 0818926013215
Application # 505G(a)(3)
SPL Set ID afda8ca4-1196-527a-e053-2995a90af9f1
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 2020-09-01
Route TOPICAL
Dosage form SHAMPOO
Substance OATMEAL
Quick answers
  • RxCUI (RxNorm): 2396990
Why two NDCs? The FDA registers this code as 10738-162-23 — 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 → 10738-0162-23. 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 Non-Standardized Food Allergenic Extract class.

Pharmacologic class Non-Standardized Food Allergenic Extract, Non-Standardized Plant Allergenic Extract
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

🧪 What is this product?

This is a topical shampoo containing colloidal oatmeal, an over-the-counter product marketed under FDA's monograph rules for skin care. Colloidal oatmeal is commonly used in cleansing products for its soothing and moisturizing properties on irritated or itchy skin. The product is designed to be applied to the scalp and hair as a wash, with the oatmeal functioning as the active ingredient intended to help calm discomfort associated with conditions like eczema.

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
10738-0162-23 You're viewing this Main listing 355 mL in 1 BOTTLE 2020-09-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Eczema Itch Relief Wash and Shampo 15 mg/mLthis 10738-0162-23 Genuine 355 ml — — FDA listed —
Eczema Fast Healing Body Wash 15 mg/mL 10738-0205-63 Genuine 473 ml — — FDA listed —
Childs Farm Eczema Moisturizing Cream 15 mg/mL 83244-0001-01 Childs 250 ml — — Discontinued —
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

🏛️
2020
On the market since
Sep 2020
📍
2026
Currently FDA-listed
6 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 ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • UNII P0M7O4Y7YD
    A plant extract from calendula flowers, traditionally used in formulations. It typically serves as a botanical ingredient that may provide color, fragrance, or skin-conditioning properties to topical products.
  • UNII FGL3685T2X
    Chamomile is a plant extract used in medications as a flavoring agent and for its mild soothing properties in formulations. It helps improve taste and aroma of the medicine.
  • UNII 5OCF3O11KX
    A plant-derived surfactant made from coconut oil. It helps mix oil and water ingredients together in the formulation and can improve how the medicine spreads or feels on the skin.
  • UNII 329M3829G2
    A sulfur-containing cleansing compound derived from lauric acid. It acts as a surfactant and emulsifier, helping to mix oil and water-based ingredients and improve how the medicine spreads or dissolves in the formulation.
  • UNII 1L0VKZ185E
    A plant-derived ingredient from horsetail grass. It may be used as a natural filler or texture agent in herbal formulations.
  • UNII 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII 72O054U628
    Lemon peel is a natural plant material from citrus fruit used as a flavoring agent and colorant in medicines. It adds tartness and a pale yellow tint to make the medication more pleasant to taste and look at.
  • UNII CUQ3A77YXI
    Panax ginseng root is a plant extract traditionally used in herbal preparations. In medications, it may serve as an active botanical ingredient or be included for flavoring and as a natural preservative or binder in formulations.
  • UNII WV9CM0O67Z
    Panthenol is a humectant and skin-conditioning agent derived from pantothenic acid. It's added to medicines to help retain moisture and soothe skin irritation.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII 0L414VCS5Y
    A synthetic polymer used as a film-former and conditioning agent. It helps create a protective coating on hair or skin surfaces and improves texture and manageability in topical formulations.
  • UNII 065C5D077J
    Sage is a natural plant extract used in medicines as a flavoring agent and preservative. It may help mask bitter tastes and extend shelf life in certain formulations.
  • UNII 55X04QC32I
    A strong alkaline chemical used to adjust and maintain the pH balance of liquid medicines. It helps keep the medicine stable and ensures it stays effective during storage.
  • UNII D0Y70F2B9J
    A synthetic detergent and surfactant derived from fatty acids. It reduces surface tension in formulations to help with mixing, emulsifying, and creating foams or dispersions in topical products.
  • UNII I39GGJ23HV
    A synthetic cleaning agent derived from lauric acid. It acts as a surfactant and emulsifier in medicines, helping blend oil and water-based ingredients and improve how the medicine dissolves and spreads in the body.
  • 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.

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

The official label also statesAcrylates Copolymer, Aloe Barbadensis (Aloe Vera) Leaf Juice*, Calendula Officinalis Flower Extract, Chamomilla Recutita (Matricaria) Flower Extract, Citrus Limon (Lemon) Fruit Extract, Cocamidopropyl Betaine, Disodium 2-Sulfolaurate, Equisetum Arvense (Horsetail) Extract, Ethylhexylglycerin, Glycerin, Panax Ginseng Root Extract, Panthenol (Vitamin B5), Phenoxyethanol, Polyquaternium-7, Salvia Officinalis (Sage) Leaf Extract, Sodium Hydroxide, Sodium Lauryl Sulfoacetate, Sodium Methyl 2-Sulfolaurate, Water. *Certified Organic Ingredient - Mayacert Certifier

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

LabelerGenuine Virgin Aloe Corporation
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code10738
First marketedSep 2020
Product typeHuman Otc Drug
Portfolio29 products on file
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 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 19 words ▾

Uses Temporarily protects and helps relieve minor skin irritation and itching due to: •eczema •rashes •poison ivy •insect bites

⏱️ Dosage and Administration 32 words ▾

Directions Dispense a dime to quarter-sized amount into palm, gently massage onto wet skin and hair. Rinse and towel dry. For extra cleansing, allow to sit for 30 seconds and then rinse.

⚠️ Warnings 91 words ▾

Warnings For external use only When using this product • patch test before use • Keep out of eyes. If contact occurs, rinse eyes thoroughly with water. Stop use and ask a doctor if • condition worsens • symptoms last for more than 7 days, or clear and occur again in a few days Do not use • on deep puncture wounds • on animals • on bites • on serious burns Keep out of reach of children.

If swallowed get medical help and contact a Poison Control Center right away.

🧪 Active Ingredient 5 words ▾

Active Ingredient Colloidal Oatmeal 1.5%

🧪 Inactive Ingredients 62 words ▾

Ingredients Acrylates Copolymer, Aloe Barbadensis (Aloe Vera) Leaf Juice*, Calendula Officinalis Flower Extract, Chamomilla Recutita (Matricaria) Flower Extract, Citrus Limon (Lemon) Fruit Extract, Cocamidopropyl Betaine, Disodium 2-Sulfolaurate, Equisetum Arvense (Horsetail) Extract, Ethylhexylglycerin, Glycerin, Panax Ginseng Root Extract, Panthenol (Vitamin B5), Phenoxyethanol, Polyquaternium-7, Salvia Officinalis (Sage) Leaf Extract, Sodium Hydroxide, Sodium Lauryl Sulfoacetate, Sodium Methyl 2-Sulfolaurate, Water. *Certified Organic Ingredient - Mayacert Certifier

🎯 Purpose 3 words ▾

Purpose Skin Protectant

📄 Do Not Use 18 words ▾

Do not use • on deep puncture wounds • on animals • on bites • on serious burns

📄 When Using This Product 22 words ▾

When using this product • patch test before use • Keep out of eyes. If contact occurs, rinse eyes thoroughly with water.

📄 Stop Use and Ask a Doctor If 27 words ▾

Stop use and ask a doctor if • condition worsens • symptoms last for more than 7 days, or clear and occur again in a few days

📄 Keep Out of Reach of Children 19 words ▾

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

📄 Questions or Comments 5 words ▾

Questions? 1-800-279-7282 M-F 8am-4pm PST

📄 Package Label / Principal Display Panel 2 words ▾

label wash

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 Eczema Itch Relief Wash and Shampo (this brand).

Top reported reactions

Rash2
Anaemia1
Aplastic Anaemia1
Asthenia1
Bile Duct Stenosis1
Cholangiocarcinoma1
Death1

Age at onset

Adult2

Reporter sex

11 reports
Male · 50%
Female · 50%

Serious outcomes

Hospitalization3
Life-threatening1
Death1
Reports over time (by year) — tap or hover for the count & year
2021 2022 2024 2026 2 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 Genuine Virgin Aloe Corporation. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Genuine Virgin Aloe 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.
← 10738-0161-45 · Genujine 10738-0168-40 · Genuine →
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.