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All Over Colloidal Oatmeal 1 g/100g Ointment, 57 g — NDC 73088-0302-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

All Over Colloidal Oatmeal 1 g/100g Ointment, 57 g — NDC 73088-302-02 (Billing 73088-0302-02)

by Tubby Todd · 57 g in 1 TUBE

This is a package of 57 g of All Over Colloidal Oatmeal 1 g/100g Ointment from Tubby Todd, marketed since Apr 2021 and currently FDA-listed. It is the main listing for this product, which comes in 9 package sizes.

NDC 73088-0302-02
🏷️ FDA NDC (as labeled) 73088-302-02 billing pads the product segment with a zero
This package
Contains57 g Pack sizes9 compare ↓
Main listing for product 73088-302 · Also comes in: 5 g 73088-302-05 10 g 73088-302-10 15 g 73088-302-15 28 g 73088-302-03 99 g 73088-302-35 113 g 73088-302-14 227 g 73088-302-08 227 g 73088-302-18
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Oct 1, 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 73088-302-02 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
73088 labeler · 302 product · 02 package
Package marketed since
Apr 20, 2021
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 7308830202 2
FDA record last changed
Oct 1, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 73088-302-02
Product NDC 73088-302
11-digit billing NDC 73088030202
Application # M016
SPL Set ID e37b225d-c7f7-111e-e053-2995a90a72b8
Established class (EPC) Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract
Physiologic effect Cell-mediated Immunity; Increased Histamine Release
Chemical class Allergens; Dietary Proteins; Grain Proteins; Plant Proteins
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-04-20
Route TOPICAL
Dosage form OINTMENT
Substance OATMEAL
Why two NDCs? The FDA registers this code as 73088-302-02 — 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 → 73088-0302-02. 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?

All Over Colloidal Oatmeal is a topical ointment containing finely ground oatmeal as its active ingredient. It is marketed as an over-the-counter monograph product, meaning it is sold under FDA's established rules for this category of skin-care product. Colloidal oatmeal is commonly used in products applied to the skin to help soothe irritation and dryness. This ointment is intended for application directly to affected areas of the skin.

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: 5 g 10 g 15 g 28 g 99 g 113 g 227 g 227 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
73088-0302-02 You're viewing this Main listing 57 g in 1 TUBE 2021-04-20 — Active
73088-0302-08 73088-302-08 227 g in 1 JAR 2021-04-20 — Active
73088-0302-35 73088-302-35 99 g in 1 JAR 2021-04-20 — Active
73088-0302-03 73088-302-03 28 g in 1 JAR 2024-12-22 — Active
73088-0302-05 73088-302-05 5 g in 1 PACKET Sample 2024-12-22 — Active
73088-0302-10 73088-302-10 10 g in 1 PACKET Sample 2024-12-22 — Active
73088-0302-15 73088-302-15 15 g in 1 TUBE 2024-12-22 — Active
73088-0302-18 73088-302-18 227 g in 1 TUBE 2024-12-22 — Active
73088-0302-14 73088-302-14 113 g in 1 TUBE 2026-09-21 — Active

Pack size FAQ

What quantity is in this package?
This package contains 57 g — 57 g in 1 tube.
How does this package differ from NDC 73088-0302-05?
Both are All Over Colloidal Oatmeal 1 g/100g Ointment — the drug itself is identical. This page's package is the 57 g one, while NDC 73088-0302-05 is the 5 g package.
What NDC number is used to bill for this package of All Over Colloidal Oatmeal 1 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
All Over 1 g/100gthis 73088-0302-02 Tubby 57 g — — FDA listed —
All Over Lavender Rosemary 1 g/100g 73088-0303-08 Tubby 227 g — — FDA listed —
Barrier Balm 1 g/100g 73088-0305-01 Tubby 14 g — — FDA listed —
Babo Botanicals Sensitive Baby Healing 10 mg/g 79265-8655-01 Babo 1 jar — — FDA listed —
EczemaHoneyBodyLotion 1 g/100g 62742-4234-01 Allure 226.79 g — — FDA listed —
Eczema Relief Cream 1 g/100g 71521-0025-15 Lavior 15 g — — FDA listed —
Baby Eczema Moisturizing Cream 1 g/100g 87781-0003-01 Foshan 80 g — — FDA listed —
Olay Ultimate Sensitive Colloidal Oatmeal Skin Protectant Moisturizer Fragrance Free 1 g/100g 69423-0743-48 The 1 jar — — FDA listed —
Honest Eczema Balm 1 g/100g 69366-0503-20 The 1 jar — — Discontinued —
Honest Eczema Cream 1 g/100g 69366-0504-19 The 200 g — — FDA listed —
Eczema Hand Relief 1 g/100g 61328-0010-00 Skinfix, 90 g — — FDA listed —
Tagrid Eczema Cream Colloidal Oatmeal 1% 1 g/100g 85384-0024-01 TAGRID 56.7 g — — FDA listed —
Puriya Eczema Cream 1 g/100g 84711-0002-04 IPC 113 g — — FDA listed —
Avene XERACALM Eczema Calming Relief Balm 1 g/100g 64760-0777-01 Pierre 100 g — — FDA listed —
EczeNourish Eczema and Psoriasis Soothing Oat 1 g/100g 51642-0074-42 Vanguard 99 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

🏛️
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 SDS87L369F
    A natural oil extracted from avocado fruit. It's used as an emollient and skin-conditioning agent in topical formulations to help soften and smooth the product's texture.
  • UNII 2ZA36H0S2V
    Beeswax is a natural wax produced by honeybees. In medicines, it works as a coating agent and thickener to control how fast the drug dissolves and improve the product's texture and appearance.
  • UNII W2ZU1RY8B0
    A plant extract from green tea leaves. It's used as an antioxidant ingredient to help preserve the medicine and maintain its stability during storage.
  • UNII C9H2L21V7U
    A fat derived from coconut or palm oil containing shorter fatty acid chains. It serves as a solvent and carrier to help dissolve or suspend active ingredients, improving absorption and stability in liquid formulations.
  • UNII 936JST6JCN
    Cetyl alcohol is a waxy, fatty substance derived from plant or animal sources. It acts as an emulsifier and thickener in medicines, helping blend oil and water components and giving products a smooth, creamy texture.
  • UNII YY7C30VXJT
    A natural plant extract from cucumber that adds flavor and freshness to medicines. It may also serve as a moisturizing agent or mild preservative in topical or oral formulations.
  • 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 UDR641JW8W
    A plant-derived oil from jojoba seeds that has been broken down into smaller components. It acts as an emollient and skin-conditioning agent to help soften and smooth the product's texture.
  • UNII 5N1WD9784U
    A plant-derived ingredient from honeysuckle flowers, used as a natural flavoring or fragrance component to improve taste or aroma in the medicine.
  • UNII 4465L2WS4Y
    A plant extract from Japanese honeysuckle flowers used as a natural flavoring and fragrance ingredient in medicines. It may also help preserve the product and add pleasant taste or aroma.
  • UNII I629I3NR86
    A natural flavoring derived from mango fruit, used to add taste and aroma to medicines. It helps mask bitter or unpleasant flavors, making the medication more pleasant to take.
  • UNII 5965N8W85T
    Propanediol is a clear liquid organic compound derived from vegetable sources or synthesized chemically. It acts as a humectant to retain moisture, a solvent to dissolve active ingredients, and a preservative booster in liquid medications and supplements.
  • UNII R85W246Z1C
    A yeast-derived substance made from broken-down Saccharomyces cerevisiae cells. It is used as a natural humectant and moisturizing agent to help keep medicines and supplements stable and prevent them from drying out.
  • UNII 4ELV7Z65AP
    Stearic acid is a fatty acid derived from plant or animal sources. It acts as a binder and lubricant in tablets and capsules, helping them hold together and flow smoothly during manufacturing.
  • UNII 2KR89I4H1Y
    Stearyl alcohol is a waxy, fatty substance derived from natural oils or made synthetically. It acts as an emulsifier and thickener in medicines, helping mix ingredients together and give the product the right texture.
  • 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.

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

The official label also statesBeeswax, Camellia Sinensis Leaf Extract*, Caprylic/Capric Triglyceride, Cetyl Alcohol, Cucumis Sativus (Cucumber), Fruit Extract*, Glycerin, Jojoba Esters, Lonicera Caprifolium, (Honeysuckle) Flower Extract, Lonicera Japonica (Honeysuckle) Flower Extract, Mangifera Indica (Mango) Fruit Extract*, Persea Gratissima (Avocado) Fruit Extract*, Propanediol, Saccharomyces Ferment Filtrate, Stearic Acid, Stearyl Alcohol, Water *Organic ingredient

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

LabelerTubby Todd
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code73088
First marketedApr 2021
Product typeHuman Otc Drug
Portfolio12 products on file

More NDCs from Tubby Todd labeler code 73088

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 15 words ▾

Uses Temporarily protects and helps relieve minor skin irritation and itching due to: Eczema Rashes

⏱️ Dosage and Administration 4 words ▾

Directions Apply as needed

⚠️ Warnings 49 words ▾

Warnings For External Use Only When using this product do not use near eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if condition worsens. symptoms may last more than 7 days or clear up and occur again within a few days

📦 Storage and Handling 17 words ▾

Other Information Do not use if quality seal is broken or missing Protect from excessive heat (40°C/104°F)

🧪 Active Ingredient 5 words ▾

Active Ingredients Colloidal Oatmeal 1%

🧪 Inactive Ingredients 50 words ▾

Inactive ingredients Beeswax, Camellia Sinensis Leaf Extract*, Caprylic/Capric Triglyceride, Cetyl Alcohol, Cucumis Sativus (Cucumber), Fruit Extract*, Glycerin, Jojoba Esters, Lonicera Caprifolium, (Honeysuckle) Flower Extract, Lonicera Japonica (Honeysuckle) Flower Extract, Mangifera Indica (Mango) Fruit Extract*, Persea Gratissima (Avocado) Fruit Extract*, Propanediol, Saccharomyces Ferment Filtrate, Stearic Acid, Stearyl Alcohol, Water *Organic ingredient

🎯 Purpose 3 words ▾

Purpose Skin Protectant

📄 Keep Out of Reach of Children 18 words ▾

Keep out of reach of children. If swollowed, seek medical advice or contact a Poison Control Center immediately.

📄 Questions or Comments 8 words ▾

Questions or comments? Call us at (619) 894-6560

📄 Package Label / Principal Display Panel 6 words ▾

All Over Ointment OTC 8oz Tube

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 Colloidal Oatmeal — the ingredient across all brands.

Top reported reactions

Pruritus38
Rash37
Fatigue17
Pain16
Dizziness15
Nausea15
Arthralgia14

Age at onset

Adult17
Elderly33

Reporter sex

262 reports

Serious outcomes

Life-threatening10
Disabling4
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 33 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 Tubby Todd. 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 8 other package presentations of this same product, including 5 g (73088-0302-05), 10 g (73088-0302-10), 15 g (73088-0302-15). 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?
Tubby Todd 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.
← 73088-0301-14 · Tubby 73088-0303-08 · Tubby →
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.