Home › NDC Lookup › Ingredients › Dimethicone › 72288-0619-34
Daily Moisturizing Dimethicone 13 mg/g Lotion, 227 g — NDC 72288-0619-34 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Daily Moisturizing Dimethicone 13 mg/g Lotion, 227 g — NDC 72288-619-34 (Billing 72288-0619-34)

by Amazon.com Services LLC · 227 g in 1 TUBE

This is a package of 227 g of Daily Moisturizing Dimethicone 13 mg/g Lotion from Amazon.com Services LLC, no longer marketed (first marketed Apr 2018), no longer in the FDA NDC Directory. It is the main listing for this product, which comes in 2 package sizes.

NDC 72288-0619-34
🏷️ FDA NDC (as labeled) 72288-619-34 billing pads the product segment with a zero
This package
Contains227 g Pack sizes2 compare ↓
Main listing for product 72288-619 · Also comes in: 532 g 72288-619-44
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ 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 72288-619-34 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
72288 labeler · 619 product · 34 package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0038000008689
FDA record last changed
Jul 24, 2026
⚠️
Other active recalls for Dimethicone (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Jun 11, 2026 — Failed Impurities/Degradation Specifications; Formaldehyde levels exceeded specification. (BioMed Laboratories, LLC.) · FDA recall D-0663-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗
⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 72288-619-34
Product NDC 72288-619
11-digit billing NDC 72288061934
RxCUI 891710
UNII 92RU3N3Y1O
UPC 0038000008689
Application # M016
SPL Set ID 2762cc82-e40c-4751-a74e-14804ea4b5f2
Physiologic effect Skin Barrier Activity
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm
Marketing start 2018-04-25
Route TOPICAL
Dosage form LOTION
Substance DIMETHICONE
Quick answers
  • RxCUI (RxNorm): 891710
Why two NDCs? The FDA registers this code as 72288-619-34 — 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 → 72288-0619-34. 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 Other ectoparasiticides, incl. scabicides class.

Drug family (ATC) Other ectoparasiticides, incl. scabicides
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 an over-the-counter moisturizing lotion applied to the skin. It contains dimethicone, a silicone-based ingredient commonly used in skincare products to help soften and protect the outer layer of skin. Dimethicone functions as a skin protectant and is typically included in moisturizers and lotions intended for daily skin care. This product is marketed under FDA's monograph rule for over-the-counter skin protectants rather than through individual product approval.

Supplement & herbal interactions

Some supplements/herbs that may interact with Dimethicone — tap one for details:

Dimethylsulfoxide (dmso)Moderate Turpentine OilModerate AlchemillaMinor
🌿 Every supplement checked against Dimethicone (3 interactions) — ranked by severity →
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: 532 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
72288-0619-34 You're viewing this Main listing 227 g in 1 TUBE 2018-04-25 — Discontinued by firm
72288-0619-44 72288-619-44 532 g in 1 BOTTLE, PLASTIC 2018-04-25 — Active

You're viewing the smallest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 227 g — 227 g in 1 tube.
How does this package differ from NDC 72288-0619-44?
Both are Daily Moisturizing Dimethicone 13 mg/g Lotion — the drug itself is identical. This page's package is the 227 g one, while NDC 72288-0619-44 is the 532 g package.
What NDC number is used to bill for this package of Daily Moisturizing Dimethicone 13 mg/g 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
Daily Moisturizing 13 mg/g 00363-0619-18 Walgreen 71 g — — Discontinued —
Daily Moisturizing 13 mg/mL 11822-0619-01 Rite 354 ml — — Discontinued —
Oatmeal 13 mg/mL 21130-0898-32 Better 354 ml — — FDA listed —
Daily Moisturizing 13 mg/mL 30142-0619-44 The 532 ml — — FDA listed —
Daily Moisturizing 13.13 mg/mL 36800-0619-40 Topco 354 ml — — FDA listed —
Daily Moisturizing 13 mg/mL 41250-0619-40 Meijer, 354 ml — — FDA listed —
Daily Moisturizing 1.3 kg/100mL 55301-0619-40 Your 354 ml — — FDA listed —
Daily Moisturizing 13 mg/mL 56062-0619-34 Publix 227 ml — — Discontinued —
XtraCare Skin Relief Oatmeal Daily Moisturizing 5 mg/354mg 57337-0037-01 Rejoice 354 mg — — FDA listed —
XtraCare with cooling action Oatmeal Skin Relief Calmin 5 mg/354mg 57337-0038-01 Rejoice 354 mg — — FDA listed —
XtraCare Skin Relief Oatmeal Daily Moisturizing 3 g/227g 57337-0054-01 Rejoice 227 g — — FDA listed —
XtraCare with cooling action Oatmeal Skin Relief Calmin 3 g/227g 57337-0055-01 Rejoice 227 g — — FDA listed —
Oatmeal Skin Relief Calming . 8oz 3 g/227g 57337-0100-01 Rejoice 227 g — — FDA listed —
XtraCare Oatmeal Daily Moisturizing 8 oz 1.3 g/100g 57337-0138-01 Rejoice 227 g — — FDA listed —
XtraCare Oatmeal Daily Moisturizing 8 oz 1.3 g/100g 57337-0139-01 Rejoice 227 g — — FDA listed —
Harmon Daily Moisturzier 13 mg/mL 63940-0074-03 HARMON 85 ml — — FDA listed —
Daily Moisturizing 13.13 mg/mL 64024-0619-44 Aldi, 532 ml — — FDA listed —
Daily Moisturizing 1.3 kg/100mL 69842-0771-40 CVS 354 ml — — Discontinued —
Daily Moisturizing 1.3 kg/100mL 71141-0619-44 Lidl 532 ml — — FDA listed —
Daily Moisturizing 13 mg/gthis 72288-0619-34 Amazon.com 227 g — — Discontinued —
Daily Moisturizing 13 mg/mL 72476-0619-40 Retail 354 ml — — 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

🏛️
2018
On the market since
Apr 2018
📍
2026
Currently FDA-listed
8 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 LKG8494WBH
    Benzyl alcohol is a clear liquid used as a preservative and solvent in medicines. It helps prevent bacterial and fungal growth and dissolves other ingredients to create uniform 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 OM9573ZX3X
    A synthetic compound used as an antistatic agent and conditioner in solid dosage forms. It reduces friction and helps powders flow smoothly during manufacturing and tablet compression.
  • 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 8CRQ2TH63M
    Isopropyl palmitate is an oily liquid derived from palm oil. It acts as an emollient and lubricant in medicines, helping soften the skin or improve how the product spreads and flows.
  • UNII 3UVP41R77R
    Avena sativa kernel oil is a natural oil extracted from oat seeds. It's used in medicines as an emollient and skin-conditioning agent to help soften and moisturize the product's texture.
  • UNII 4T6H12BN9U
    Petrolatum is a purified mineral oil-based jelly derived from petroleum. In medicines, it acts as an emollient, lubricant, and moisture barrier to soften skin, reduce friction, and help prevent water loss from formulations.
  • UNII 451W47IQ8X
    Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.
  • 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.

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

The official label also stateswater, glycerin, distearyldimonium chloride, petrolatum, isopropyl palmitate, cetyl alcohol, Avena sativa (oat) kernel flour, benzyl alcohol, sodium chloride

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

LabelerAmazon.com Services LLC
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code72288
First marketedApr 2018
Product typeHuman Otc Drug
Portfolio345 products on file

More NDCs from Amazon.com Services LLC labeler code 72288

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 🤒 Adverse Reactions 🧪 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 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 22 words ▾

Use helps prevent and temporarily protects chafed, chapped, or cracked skin helps protect from the drying effects of wind and cold weather

⏱️ Dosage and Administration 4 words ▾

Directions apply as needed

⚠️ Warnings 5 words ▾

Warnings For external use only

🤒 Adverse Reactions 39 words ▾

ADVERSE REACTIONS SECTION Made in USA of domestic and foreign materials. DISTRIBUTED BY: Amazon.com Services LLC Seattle, WA 98109 1-877-485-0385 ©2026 Amazon.com, Inc., or its affiliates. All rights reserved. www.amazon.com/amazonessentials PLASTIC BOTTLE Widely Recyclable Empty & Replace Cap how2recycle.info

🧪 Active Ingredient 4 words ▾

Active ingredient Dimethicone 1.3%

🧪 Inactive Ingredients 20 words ▾

Inactive ingredients water, glycerin, distearyldimonium chloride, petrolatum, isopropyl palmitate, cetyl alcohol, Avena sativa (oat) kernel flour, benzyl alcohol, sodium chloride

🎯 Purpose 3 words ▾

Purpose Skin protectant

📄 Do Not Use 12 words ▾

Do not use on deep or puncture wounds animal bites serious burns

📄 When Using This Product 9 words ▾

When using this product do not get into eyes

📄 Stop Use and Ask a Doctor If 25 words ▾

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

📄 Keep Out of Reach of Children 19 words ▾

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

📄 Package Label / Principal Display Panel 59 words ▾

Principal Display Panel amazon essentials Oatmeal Skin Protectant Lotion Moisturizing Formulated without fragrance Skin protectant Compare to Aveeno ® Daily Moisturizing Lotion* 18 FL OZ (1.12 PT) 532 mL image description image description

principal display panel amazon basics daily moisturizing oatmeal lotion Skin Protectant Fragrance Free Compare to Aveeno Daily Moisturizing Lotion 18 FL OZ (532 mL) image description

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 No longer marketed (per FDA listing data)
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 532 g (72288-0619-44). 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?
Amazon.com Services 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.
← 72288-0618-01 · AMAZON.COM 72288-0623-14 · Amazon.com →
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.