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Santal Suede Hand Sanitizer Ethyl Alcohol 70 mL/100mL Liquid, 18 mL — NDC 87361-0008-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Santal Suede Hand Sanitizer Ethyl Alcohol 70 mL/100mL Liquid, 18 mL — NDC 87361-008-01 (Billing 87361-0008-01)

by PEACH LAYNE, LLC · 18 mL in 1 BOTTLE

This is a package of 18 mL of Santal Suede Hand Sanitizer Ethyl Alcohol 70 mL/100mL Liquid from PEACH LAYNE, LLC, marketed since Jun 2026 and currently FDA-listed. It is this product's only package size.

NDC 87361-0008-01
🏷️ FDA NDC (as labeled) 87361-008-01 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 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 87361-008-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
87361 labeler · 008 product · 01 package
Package marketed since
Jun 15, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0840530604459
FDA record last changed
Jul 24, 2026
⚠️
Other active recalls for Ethyl Alcohol (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 · May 23, 2025 — Subpotent product: Product has cloudy appearance and tested below assay label claim for 70% Ethyl Alcohol (Consumer Product Partners, LLC) · FDA recall D-0458-2025
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 87361-008-01
Product NDC 87361-008
11-digit billing NDC 87361000801
RxCUI 1041849
UNII 3K9958V90M
UPC 0840530604459
Application # 505G(a)(3)
SPL Set ID 55712a8b-e633-2427-e063-6294a90a7c5a
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-06-15
Route TOPICAL
Dosage form LIQUID
Substance ALCOHOL
Quick answers
  • RxCUI (RxNorm): 1041849
Why two NDCs? The FDA registers this code as 87361-008-01 — 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 → 87361-0008-01. 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.

RxNorm drug class

This medicine belongs to the Other antiseptics and disinfectants class.

Drug family (ATC) Other antiseptics and disinfectants, Antidotes, Nerve depressants
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

📗 Our plain-language guide HelloPharmacist
  • It depends on the product. Hand sanitizers and wipes help reduce bacteria on your skin, and alcohol pads prepare skin before an injection. A separate injected form is used by heart...
  • Most directions say to cover all surfaces of your hands and rub until dry. Sprays and wipes follow similar steps. Check your product's label, since directions differ a bit between...
  • Children under 6 should use hand sanitizer only with adult supervision to avoid swallowing. Keep all products out of reach of children. If someone swallows it, get medical help or...
  • Stop using it and ask a doctor if you get irritation and redness, or if your condition lasts more than 72 hours. Avoid broken skin and keep it out of your eyes. If it gets in your...
📖 Read our full Alcohol guide →

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 mLPer 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
87361-0008-01 You're viewing this Main listing 18 mL in 1 BOTTLE 2026-06-15 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Ethyl Rubbing Alcohol 70 mL/100mL 70000-0020-01 Cardinal 473 ml $0.004 — Availability likely —
Ethyl alcohol 70 mL/100mL 70677-1220-01 Strategic 473 ml $0.004 — Availability likely —
DOP Ethyl Alcohol 70% 70 mL/100mL 51048-0048-16 Omega 473 ml — — FDA listed —
EnMotion Foam Hand Sanitizer 70 mL/100mL 54622-0120-01 Georgia-Pacific 1000 ml — — FDA listed —
Pacific Blue Select Foam Hand Sanitizer, Fragrance Free, Dye Free 70 mL/100mL 54622-0311-01 Georgia-Pacific 24 bottles — — FDA listed —
Hand Sanitizer w/ Carabiner (Strawberry Scented) 2oz Bonus pack 70 mL/100mL 57337-0094-01 Rejoice 2 bottles — — FDA listed —
Hand Sanitizer 1.8 oz Strawberry Scented 70 mL/100mL 57337-0112-01 Ningbo 53 ml — — FDA listed —
Hand Sanitizer Antibacterial Vitamin E 70 mL/100mL 57337-0121-01 Ningbo 177 ml — — FDA listed —
Watermelon Whirl Hand Sanitizer 70 mL/100mL 87361-0004-01 PEACH 1 bottle — — FDA listed —
Quik-Care 70 mL/100mL 47593-0491-38 Ecolab 500 ml — — Discontinued —
Hand Sanitizer w/ Carabiner (Watermelon Scented) 2oz Bonus pack 70 mL/100mL 57337-0096-01 Rejoice 2 bottles — — FDA listed —
Ethyl Rubbing Alcohol 70 mL/100mL 59779-0164-43 CVS 473 ml — — FDA listed —
Ethyl Rubbing Alcohol 70 mL/100mL 55301-0876-43 Your 473 ml — — FDA listed —
Hand Sanitizer w/ Carabiner (Lemon Scented) 2oz Bonus pack 70 mL/100mL 57337-0095-01 Rejoice 2 bottles — — FDA listed —
Ethyl Rubbing Alcohol 70 mL/100mL 72288-0876-43 Amazon.com 473 ml — — FDA listed —
Vanilla Salt Air Hand Sanitizer 70 mL/100mL 87361-0003-01 PEACH 1 bottle — — FDA listed —
enMotion Foam High Frequency Use 70 mL/100mL 54622-0486-01 Georgia-Pacific 1000 ml — — FDA listed —
Hand Sanitizer Original 1.8 oz 70 mL/100mL 57337-0117-01 Ningbo 53 ml — — FDA listed —
Ops 70 Percent Alcohol Foaming Skin Sanitizer 70 mL/100mL 79016-0101-12 Archer 1000 ml — — FDA listed —
Rubbing 70 mL/100mL 50804-0876-43 Perrigo 473 ml — — FDA listed —
Hand sanitizer 16.9oz with vitamin E 70 mL/100mL 55319-0118-01 Midwood 500 ml — — FDA listed —
Hand Sanitizer Vitamin E and Aloe Vera 70 mL/100mL 57337-0116-01 Ningbo 236 ml — — FDA listed —
Hand Sanitizer Vitamin E 70 mL/100mL 57337-0119-01 Ningbo 2 bottles — — FDA listed —
Berry Bougie Hand Sanitizer 70 mL/100mL 87361-0001-01 PEACH 1 bottle — — FDA listed —
INSTANT HAND SANITIZER Classic 70 mL/100mL 52000-0434-01 Universal 1000 ml — — FDA listed —
Hand Sanitizer 8 oz. Vitamin E 70 v/v 70 mL/100mL 57337-0115-01 Ningbo 236 ml — — FDA listed —
Hand Sanitizer Antibacterial Vitamin E 2 oz. 2 pk 70 mL/100mL 57337-0118-01 Ningbo 2 bottles — — FDA listed —
Rubbing 70 mL/100mL 41163-0876-43 United 473 ml — — FDA listed —
microdot Hand Sanitizing Wipe 70 mL/100mL 52422-0622-06 Cambridge 563.91 ml — — FDA listed —
Ethyl Rubbing Alcohol 70 mL/100mL 00363-0876-43 Walgreen 473 ml — — FDA listed —
Ethyl Rubbing Alcohol 70 mL/100mL 70677-0056-01 STRATEGIC 473 ml — — Discontinued —
Mellow Hand Sanitizer Aloe 70 mL/100mL 77725-0005-17 L.e.d. 500 ml — — FDA listed —
Black Ops 70 Percent Alcohol Foaming Skin Sanitizer 70 mL/100mL 79016-0102-12 Archer 1000 ml — — FDA listed —
Ethyl Alcohol 70 mL/100mL 79903-0283-16 Walmart 473 ml — — FDA listed —
Hand Sanitizer 1.8 oz Antiseptic 70 mL/100mL 57337-0107-01 REJOICE 1 bottle — — FDA listed —
Hand Sanitizer 1.8 oz Lemon Ice 70 mL/100mL 57337-0110-01 Ningbo 53 ml — — FDA listed —
Hand Sanitizer Vitamin E and Aloe Vera 2 oz. 2 pk 70 mL/100mL 57337-0114-01 Ningbo 2 bottles — — FDA listed —
Hand Sanitizer Antibacterial Vitamin E 70 mL/100mL 57337-0120-01 Ningbo 500 ml — — FDA listed —
Hand Sanitizer Antibacterial Vitamin E 70 mL/100mL 57337-0122-01 Ningbo 1000 ml — — FDA listed —
Palma Hydrating Hand Sanitizing Serum 70 mL/100mL 81286-0102-11 UNITRADE 60 ml — — Discontinued —
Ethyl Alcohol 70 mL/100mL 11344-0876-43 Nice-Pak 473 ml — — FDA listed —
Alcohol 70 mL/100mL 68196-0602-68 Sam's 2000 ml — — FDA listed —
Rio Glow Hand Sanitizer 70 mL/100mL 87361-0002-01 PEACH 1 bottle — — FDA listed —
Rubbing 70 mL/100mL 00869-0876-43 Nice-Pak 473 ml — — FDA listed —
Instant Hand Sanitizer 2oz Bonus pack 70 mL/100mL 57337-0093-01 Rejoice 59 ml — — FDA listed —
Hand Sanitizer 1.8 oz Watermelon Scented 1.8 oz. 70 mL/100mL 57337-0111-01 Ningbo 53 ml — — FDA listed —
Hand sanitizer 16.9oz with vitamin E 70 mL/100mL 75742-0029-01 Zhejiang 500 ml — — FDA listed —
Sea Salt Bergamot Hand Sanitizer 70 mL/100mL 87361-0009-01 PEACH 18 ml — — FDA listed —
Beach In A Bottle Hand Sanitizer 70 mL/100mL 87361-0005-01 PEACH 1 bottle — — FDA listed —
Bourbon Vanilla Hand Sanitizer 70 mL/100mL 87361-0010-01 PEACH 18 ml — — FDA listed —
Whipped Creme Hand Sanitizer 70 mL/100mL 87361-0007-01 PEACH 1 bottle — — FDA listed —
Santal Suede Hand Sanitizer 70 mL/100mLthis 87361-0008-01 PEACH 18 ml — — FDA listed —
Sugarcoat Hand Sanitizer 70 mL/100mL 87361-0006-01 PEACH 1 bottle — — 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
Jun 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 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 RUE8E6T4NB
    Aloe vera leaf juice is a clear gel extracted from aloe vera plant leaves. It's used in medicines as a lubricant, emollient, and preservative to soothe skin contact and help keep the product stable.
  • UNII LU49E6626Q
    A synthetic organic compound used as a pH buffer and neutralizing agent in medicines. It helps maintain the proper acidity level in liquid formulations to improve stability and comfort.
  • UNII N863NB338G
    Benzyl benzoate is a liquid organic compound used as a solvent and preservative in medicines. It helps dissolve active ingredients and can extend shelf life by preventing microbial growth in liquid formulations.
  • UNII 2R04ONI662
    Eucalyptus oil is a fragrant liquid extracted from eucalyptus tree leaves. It's used in medicines as a flavor, scent, or soothing agent in topical products and cough preparations.
  • 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 14170060AT
    A synthetic colorant used to give medicines their yellow, orange, or red appearance. It helps identify the drug and makes it visually distinctive.
  • UNII GFD7C86Q1W
    A natural oil extracted from citrus peels, (+)-limonene is used as a flavoring agent and solvent in medicines. It helps dissolve active ingredients and provides a lemon or orange taste.
  • UNII 996299PUKB
    Pinene is a natural oil compound found in pine trees and other plants. It's used in medicines as a flavoring agent and to help mask bitter or unpleasant tastes.
  • UNII F3IN55X5PO
    A plant-derived essential oil from patchouli leaves. It serves as a fragrance and flavoring agent to improve the taste and smell of the medicine.
  • UNII N9830X5KSL
    Terpinolene is a natural aromatic compound found in plants. It's used in medicines as a flavoring agent to improve taste and scent.
  • UNII 2JU6ZH6GRE
    A synthetic fragrance compound made by modifying naphthalene molecules. It's used in very small amounts to add pleasant scent to medications, making them more appealing to take.
  • 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.

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

The official label also statesInactive Ingredients Water (Aqua), Glycerin, Fragrance (parfum), Aminomethyl Propanol, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Benzyl Benzoate, Limonene,Terpinolene, Hexamethylindanopyran, Tetramethyl Acetyloctahydronaphthalenes, Eucalyptus Globulus Oil, Pogostemon Cablin Oil, Pinene.

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

LabelerPEACH LAYNE, LLC
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code87361
First marketedJun 2026
Product typeHuman Otc Drug
Portfolio10 products on file

More NDCs from PEACH LAYNE, LLC labeler code 87361

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
🎯 Indications and Usage 13 words ▾

Uses Hand sanitizer to reduce bacteria on the skin. Recommended for repeated use.

⏱️ Dosage and Administration 28 words ▾

Directions Spray enough product in your palm to thoroughly cover hands. Rub hands together briskly until dry. Children under 6 years should be supervised when using this product.

⚠️ Warnings 13 words ▾

Warnings For external use only. Flammable - keep away form fire or flame.

📦 Storage and Handling 21 words ▾

Other information · Store below 104 ℉ (40 ℃). · Avoid excessive heat or direct sunlight. · May discolor certain fabrics.

🧪 Active Ingredient 6 words ▾

Active ingredient Ethyl Alcohol 70% v/v

🧪 Inactive Ingredients 28 words ▾

Inactive Ingredients Water (Aqua), Glycerin, Fragrance (parfum), Aminomethyl Propanol, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Benzyl Benzoate, Limonene,Terpinolene, Hexamethylindanopyran, Tetramethyl Acetyloctahydronaphthalenes, Eucalyptus Globulus Oil, Pogostemon Cablin Oil, Pinene.

🎯 Purpose 2 words ▾

Purpose Antiseptic

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 Santal Suede Hand Sanitizer (this brand).

Top reported reactions

Drug Abuse48
Toxicity To Various Agents31
Overdose27
Intentional Overdose19
Poisoning Deliberate19
Suicide Attempt19
Completed Suicide18

Age at onset

Adolescent2
Adult30
Elderly5

Reporter sex

236 reports
Male · 61%
Female · 39%

Serious outcomes

Hospitalization99
Death74
Life-threatening10
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 23 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 PEACH LAYNE, LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
PEACH LAYNE, 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.
← 87361-0007-01 · PEACH 87361-0009-01 · PEACH →
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.