Home › NDC Lookup › Ingredients › Diphenhydramine Hydrochloride And Zinc A... › 59555-0002-19
Industrial Itch and Pain Relief DIPHENHYDRAMINE HYDROCHLORIDE and Zinc Acetate 20 mg/mL; 1 mg/mL Liquid, 20 mL — NDC 59555-0002-19 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Industrial Itch and Pain Relief DIPHENHYDRAMINE HYDROCHLORIDE and Zinc Acetate 20 mg/mL; 1 mg/mL Liquid, 20 mL — NDC 59555-002-19 (Billing 59555-0002-19)

by R & R Lotion, Inc · 20 mL in 1 BOTTLE, WITH APPLICATOR

This is a package of 20 mL of Industrial Itch and Pain Relief DIPHENHYDRAMINE HYDROCHLORIDE and Zinc Acetate 20 mg/mL; 1 mg/mL Liquid from R & R Lotion, Inc, marketed since May 2019 and currently FDA-listed.

NDC 59555-0002-19
🏷️ FDA NDC (as labeled) 59555-002-19 billing pads the product segment with a zero
This package
Contains20 mL Pack sizes2 compare ↓
Product page 59555-0002-18 Also comes in: 1 ml 59555-002-18
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) 59555-002-19
Product NDC 59555-002
11-digit billing NDC 59555000219
RxCUI 1294589
UNII TC2D6JAD40, FM5526K07A
Application # M017
SPL Set ID 236415fc-f923-4a82-b54a-ecaf666dd2e0
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 2019-05-01
Route TOPICAL
Dosage form LIQUID
Substance DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE
Quick answers
  • RxCUI (RxNorm): 1294589
Why two NDCs? The FDA registers this code as 59555-002-19 — 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 → 59555-0002-19. 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

🧪 What is this product?

This is a topical liquid product marketed as an over-the-counter monograph drug under FDA rules for its category. It contains diphenhydramine hydrochloride, an antihistamine commonly used in topical products to help reduce itching, and zinc acetate, a mineral salt typically included in topical formulations for its astringent and skin-soothing properties. The liquid form is applied directly to the skin to address localized itch and minor discomfort.

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.
Try another pack size: 1 ml
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
59555-0002-18 59555-002-18 Main listing 1 mL in 1 PACKET 2019-05-01 — Active
59555-0002-19 You're viewing this 20 mL in 1 BOTTLE, WITH APPLICATOR 2019-05-01 — Active

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

Pack size FAQ

What quantity is in this package?
This package contains 20 mL — 20 ml in 1 bottle, with applicator.
How does this package differ from NDC 59555-0002-18?
Both are Industrial Itch and Pain Relief DIPHENHYDRAMINE HYDROCHLORIDE and Zinc Acetate 20 mg/mL; 1 mg/mL Liquid — the drug itself is identical. This page's package is the 20 mL one, while NDC 59555-0002-18 is the 1 ml package.
What NDC number is used to bill for this package of Industrial Itch and Pain Relief DIPHENHYDRAMINE HYDROCHLORIDE and Zinc Acetate 20 mg/mL; 1 mg/mL Liquid?
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
Industrial Itch and Pain Relief 20 mg/mL; 1 mg/mLthis 59555-0002-19 R 20 ml — — FDA listed —
Benadryl Extra Strength Itch Relief 1 mg/mL; 20 mg/mL 69968-0459-01 Kenvue 1 applicator — — 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

🏛️
2019
On the market since
May 2019
📍
2026
Currently FDA-listed
7 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.

What it looks like

Color White
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

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 U725QWY32X
    Povidone K30 is a synthetic polymer made from petroleum. It acts as a binder to hold tablet ingredients together and as a disintegrant to help the tablet break apart in the stomach so the medicine can be absorbed.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • 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.
  • UNII TTV12P4NEE
    Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.

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

The official label also statesPropylene Glycol, Xanthan Gum, DI Water, PVP K-30

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

LabelerR & R Lotion, Inc
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code59555
First marketedMay 2019
Product typeHuman Otc Drug
Portfolio13 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 📦 Storage and Handling 🧪 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 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 41 words ▾

Uses Temporary relieves pain and itching associated with: Insect Bites Minor Burns Minor Cuts Sunburn Minor Skin Irritations Scrapes Dries oozing and weeping of Poison Ivy, Poison Oak, and Poison Sumac Rashes due to Poison Ivy, Poison Oak, and Poison Sumac.

⏱️ Dosage and Administration 59 words ▾

Directions Do not use more than directed Hold stick stright down over infected area press tip of stick repeatedly on affect skin area until liquid flows, then dab sparingly adults and children 2 years of age and older: apply to affected area not more then 3 to 4 times daily children under 2 years of age: ask a doctor

⚠️ Warnings 92 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 avoid contact with eyes Stop use and ask doctor if conditions worsen, or do not improve within 7 days symptoms persist for 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 Poison Control Center right away.

📦 Storage and Handling 7 words ▾

Other Information Protect from excessive heat (40ºC/104ºF)

🧪 Active Ingredient 13 words ▾

Active Ingredients Purpose Diphenhydramine HCL 2% Topical Analgesic Zinc Acetate 0.1% Skin Protectant

🧪 Inactive Ingredients 10 words ▾

Inactive Ingredients Propylene Glycol, Xanthan Gum, DI Water, PVP K-30

🎯 Purpose 13 words ▾

Active Ingredients Purpose Diphenhydramine HCL 2% Topical Analgesic Zinc Acetate 0.1% Skin Protectant

📄 Do Not Use 24 words ▾

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 a Doctor Before Use If 9 words ▾

Ask doctor before use on chicken pox on measles

📄 When Using This Product 8 words ▾

When using this product avoid contact with eyes

📄 Stop Use and Ask a Doctor If 32 words ▾

Stop use and ask doctor if conditions worsen, or do not improve within 7 days symptoms persist for more than 7 days or clear up and occur again within a few days.

📄 Keep Out of Reach of Children 18 words ▾

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

📄 Questions or Comments 4 words ▾

Questions or Comments? 1-888-860-7424

📄 Package Label / Principal Display Panel 59 words ▾

PRINCIPAL DISPLAY PANEL - 20 ML Bottle Label Provides Temporary Relief from: Insect Bites Stings Cuts, Scrapes & Burns Poison Oak, Sumac & Ivy Sunburn Skin Irritation INDUSTRIAL STRENGTH ITCH & PAIN RELIEF ITCH RELIEF STICK R&R Lotion Made in USA RRlotion.com PN# ISIP-STICK .76 FL. OZ. [20ML] e Peel Here PRINCIPAL DISPLAY PANEL - 20 ML Bottle Label

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 ✓ 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 R & R Lotion, Inc. 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 1 other package presentation of this same product, including 1 ml (59555-0002-18). 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?
R & R Lotion, Inc 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.
← 59534-0002-01 · Richmond 59555-0109-10 · R →
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.