Home › NDC Lookup › Ingredients › Diphenhydramine Hcl, Zinc Acetate › 82895-0715-60
💨image loading
(from DailyMed)

Westlake Itch Relief Diphenhydramine HCl, Zinc Acetate .1 g/100mL; 2 g/100mL Spray, 59 mL — NDC 82895-715-60 (Billing 82895-0715-60)

by Westlake HB Pharma LLC · 59 mL in 1 BOTTLE, SPRAY

This is a package of 59 mL of Westlake Itch Relief Diphenhydramine HCl, Zinc Acetate .1 g/100mL; 2 g/100mL Spray from Westlake HB Pharma LLC, marketed since Oct 2023 and currently FDA-listed. It is this product's only package size.

NDC 82895-0715-60
🏷️ FDA NDC (as labeled) 82895-715-60 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 Aug 27, 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 82895-715-60 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
82895 labeler · 715 product · 60 package
Package marketed since
Oct 1, 2023
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 8289571560 4
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 82895-715-60
Product NDC 82895-715
11-digit billing NDC 82895071560
RxCUI 1053138
UNII FM5526K07A, TC2D6JAD40
Application # M017
SPL Set ID 0c416ba6-b01f-0609-e063-6294a90ae2a1
Established class (EPC) Copper Absorption Inhibitor; Histamine-1 Receptor Antagonist
Mechanism of action Histamine H1 Receptor Antagonists
Physiologic effect Decreased Copper Ion Absorption
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-10-01
Route TOPICAL
Dosage form SPRAY
Substance ZINC ACETATE; DIPHENHYDRAMINE HYDROCHLORIDE
Quick answers
  • RxCUI (RxNorm): 1053138
Why two NDCs? The FDA registers this code as 82895-715-60 — 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 → 82895-0715-60. 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 Histamine-1 Receptor Antagonist class.

Pharmacologic class Histamine-1 Receptor Antagonist
Drug family (ATC) Propionic acid derivatives, Antihistamines for topical use, Aminoalkyl ethers
How it works Histamine H1 Receptor Antagonists
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

📖 About the active ingredient: Zinc Acetate; Diphenhydramine Hydrochloride MedlinePlus · NLM
General information about the ingredient itself — the description of this specific product follows below.

Diphenhydramine is used to treat allergy and cold symptoms: sneezing runny nose red, itchy, watery eyes itching of the nose or throat Diphenhydramine is also used to treat insomnia (difficulty falling asleep or staying asleep) in adults, but should not be used to make a child sleepy. Diphenhydramine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms. Diphenhydramine is also available in combination with other medications. This monograph only includes information about the use of diphenh...

Read the full MedlinePlus article ↗
🧪 What is this product?

Westlake Itch Relief is a topical spray containing diphenhydramine hydrochloride and zinc acetate. This is an over-the-counter product marketed under FDA's monograph rules for itch-relief sprays. Diphenhydramine is an antihistamine commonly used in topical products to help reduce itching, while zinc acetate functions as an astringent and skin-soothing agent. The spray form allows direct application to affected skin areas.

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
82895-0715-60 You're viewing this Main listing 59 mL in 1 BOTTLE, SPRAY 2023-10-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Good neighbor Pharmacy Itch Relief .1 g/100mL; 2 g/100mL 46122-0572-46 AMERISOURCEBERGEN 59 ml $0.047 — Availability likely —
Itch Relief 20 mg/mL; 1 mg/mL 70000-0023-01 Cardinal 59 ml $0.047 — Availability likely —
Diphenhydramine HCl and Zinc Acetate 1.52 g/76g; .076 g/76g 00363-0215-76 Walgreen 76 g — — FDA listed —
Extra Strength Wal-Dryl Itch Relief 20 mg/mL; 1 mg/mL 00363-2177-00 WALGREEN 88 ml — — FDA listed —
Rite Aid Itch Relief 2 g/100g; .1 g/100g 11822-0647-02 Rite 59 g — — FDA listed —
Diphenhydramine HCl and Zinc Acetate 1.52 g/76g; .076 g/76g 30142-0134-27 Kroger 76 g — — Discontinued —
Diphenhydramine HCl and Zinc Acetate 1.5 g/76g; .075 g/76g 36800-0126-76 Topco 76 g — — FDA listed —
Diphenhydramine HCl and Zinc Acetate 1.52 g/76g; .076 g/76g 37808-0526-27 HEB 76 g — — FDA listed —
Diphenhydramine HCl and Zinc Acetate 1.52 g/76g; .076 g/76g 41250-0058-30 Meijer 76 g — — FDA listed —
Itch Relief 20 mg/mL; 1 mg/mL 41250-0295-20 Meijer, 59 ml — — FDA listed —
Itch Relief 1 mg/g; 20 mg/g 42507-0986-76 HY-VEE, 76 g — — FDA listed —
Diphenhydramine HCl and Zinc Acetate 1.5 g/88mL; .075 g/88mL 49035-0015-03 Wal-Mart 88 ml — — FDA listed —
GoodSense Anti-Itch 2 g/100mL; .1 g/100mL 50804-0064-02 Geiss, 59 ml — — FDA listed —
Itch Relief 20 mg/mL; 1 mg/mL 55910-0295-20 Old 59 ml — — FDA listed —
Itch Relief 1 mg/mL; 20 mg/mL 59450-0295-20 The 59 ml — — FDA listed —
Quality Choice Itch Relief .1 g/100mL; 2 g/100mL 63868-0952-02 Chain 59 ml — — FDA listed —
Best Choice Itch Relief .1 g/100mL; 2 g/100mL 63941-0259-02 Valu 59 ml — — FDA listed —
Itch Relief 1.5 g/76g; .076 g/76g 69842-0235-27 CVS 76 g — — FDA listed —
CVS Itch Relief .1 g/100mL; 2 g/100mL 69842-0952-02 CVS 59 ml — — FDA listed —
Benadryl Extra Strength Itch Cooling 20 mg/mL; 1 mg/mL 69968-0270-02 Kenvue 59 ml — — FDA listed —
Itch Relief 20 mg/mL; 1 mg/mL 72476-0295-20 Retail 059 l — — Discontinued —
Warrior First Aid Anti Itch 2 g/100mL; .1 g/100mL 72839-0647-02 Derma 59 ml — — FDA listed —
Extra Strength Itch Relief 20 mg/g; 1 mg/g 79481-0598-01 Meijer 76 g — — FDA listed —
Westlake Itch Relief .1 g/100mL; 2 g/100mLthis 82895-0715-60 Westlake 59 ml — — FDA listed —
Extra Strength Itch Relief 20 mg/g; 1 mg/g 83324-0302-27 Chain 76 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

🏛️
2023
On the market since
Oct 2023
📍
2026
Currently FDA-listed
3 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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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

LabelerWestlake HB Pharma LLC
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code82895
First marketedOct 2023
Product typeHuman Otc Drug
Portfolio2 products on file

More NDCs from Westlake HB Pharma LLC labeler code 82895

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 and Cautions ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 Ask a Doctor Before Use If 📄 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 40 words ▾

Uses for temporary relieves pain and itching due to: insect bites minor burns sunburn minor skin irritations minor cuts scrapes rashes due to poison ivy, poison oak, and poison sumac dries the oozing and weeping of poison: ivy oak sumac

⏱️ Dosage and Administration 34 words ▾

Directions do not use more often than directed adults and children 2 years and older: apply to affected area not more than 3 to 4 times daily children under 2 years: ask a doctor

⚠️ Warnings and Cautions 90 words ▾

Warnings For external use only Do not Use on large areas of the body with any other product containing diphenhydramine, even one taken by mouth Ask doctor Before use on chicken pox on measles When using this product do not get into eyes Stop Use and ask physician condition worsens symptoms last more than 7 days or clear up and occur again within a few days Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away. Warning for external use only

⚠️ Warnings 5 words ▾

Warning for external use only

🧪 Active Ingredient 12 words ▾

Active Ingredient Diphenhydramine hydrochloride 2% Topical analgesic Zinc acetate 0.1% Skin protectant

🧪 Inactive Ingredients 11 words ▾

Inactive Ingredients Purified Water, Glycerin, SD Alcohol, Povidone, Povidonee (K-30), Trolamine

🎯 Purpose 3 words ▾

Purposes Itch relief

📄 Do Not Use 20 words ▾

Do not Use on large areas of the body with any other product containing diphenhydramine, even one taken by mouth

📄 Ask a Doctor Before Use If 9 words ▾

Ask doctor Before use on chicken pox on measles

📄 When Using This Product 9 words ▾

When using this product do not get into eyes

📄 Stop Use and Ask a Doctor If 23 words ▾

Stop Use and ask physician 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 32 words ▾

Prinicpal dispaly panel Diphenhydramine hydrochloride 2% Topical analgesic Zinc acetate 0.1% Skin protectant Relieves Itch and Pain associated with insects bites & rashes due to posinon ivy Oak& sumac Principal Display Panel

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 — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 Westlake HB Pharma LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Westlake HB Pharma 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.
← 82891-0042-01 · Evereen 82895-0716-30 · Westlake →
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.