Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.
DOCTORS TOUCH Erase The Pain Lidocaine LIDOCAINE HYDROCHLORIDE 40 mg/mL Liquid, 90 mL — NDC 80045-400-00 (Billing 80045-0400-00)
by DOCTOR'S CHOICE MEDICAL, LLC · 90 mL in 1 BOTTLE
This is a package of 90 mL of DOCTORS TOUCH Erase The Pain Lidocaine LIDOCAINE HYDROCHLORIDE 40 mg/mL Liquid from DOCTOR'S CHOICE MEDICAL, LLC, marketed since Apr 2023 and currently FDA-listed. It is this product's only package size.
NDC 80045-0400-00
🏷️ FDA NDC (as labeled)
80045-400-00
billing pads the product segment with a zero
🗂️ 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 →
⚠️
Other active recalls for Lidocaine Hydrochloride (different manufacturers) — 6 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Jul 16, 2026 — Presence of Particulate Matter: Hair was found in products (Fresenius Kabi USA, LLC) · FDA recall D-0726-2026
Class II · Jun 8, 2026 — Lack of Assurance of Sterility (Asclemed USA Inc.) · FDA recall D-0658-2026
Class II · Apr 2, 2026 — Lack of Assurance of Sterility (Huons Co., Ltd.) · FDA recall D-0529-2026
Class II · Apr 2, 2026 — Lack of Assurance of Sterility (Huons Co., Ltd.) · FDA recall D-0532-2026
Class II · Nov 30, 2021 — Superpotent Drug: Minimally superpotent (Teligent Pharma, Inc.) · FDA recall D-0296-2022
Class I · Nov 30, 2021 — Superpotent Drug (Teligent Pharma, Inc.) · FDA recall D-0295-2022
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)
80045-400-00
Product NDC
80045-400
11-digit billing NDC
80045040000
RxCUI
1987647
UNII
V13007Z41A
UPC
0195893379828
Application #
M015
SPL Set ID
3dc9947b-8196-4a38-97b4-c2340ee77e0f
Established class (EPC)
Amide Local Anesthetic; Antiarrhythmic
Physiologic effect
Local Anesthesia
Chemical class
Amides
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2023-04-17
Route
TOPICAL
Dosage form
LIQUID
Substance
LIDOCAINE HYDROCHLORIDE
Quick answers
- RxCUI (RxNorm): 1987647
Why two NDCs?
The FDA registers this code as 80045-400-00 — 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 → 80045-0400-00. 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
RxNorm drug class
This medicine belongs to the Antiarrhythmic class.
Pharmacologic class
Antiarrhythmic, Amide Local Anesthetic
Drug family (ATC)
Antiarrhythmics, class Ib, Local anesthetics, Anesthetics for topical use
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.
- RxClass (NLM) · catalog refreshed Oct 1, 2026
Clinical
📗 Our plain-language guide HelloPharmacist
- Lidocaine numbs the area where it is used. Clinicians inject it for procedures. Skin products are used for pain, itching, minor burns, insect bites, hemorrhoid discomfort, and in s...
- Clean and dry the skin first, then apply as your product’s directions say. Wash your hands afterward. Don’t exceed the number of uses on the label. Ask a doctor before using a prod...
- No. Heat can increase how much lidocaine your body absorbs. Don’t bandage tightly either. Also avoid using other topical pain products at the same time.
- Can I use a heating pad with a lidocaine patch?
Patient education
Supplement & herbal interactions
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.
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
💬 Questions about LIDOCAINE HYDROCHLORIDE?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
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 system | Per mL | Per 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.
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 3, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 80045-0400-00 You're viewing this Main listing | 90 mL in 1 BOTTLE | 2023-04-17 | — | Active |
Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Lidocaine Hydrochloride 40 mg/mL 70954-0518-10 | Novitium | 1 bottle | $0.222 | AT | Availability likely | — |
| Lidocaine Hydrochloride 40 mg/mL 00054-3505-47 | Hikma | 50 ml | $0.222 | AT | Availability likely | — |
| Lidocaine Hydrochloride 40 mg/mL 00121-0972-51 | PAI | 1 bottle | $0.222 | AT | Availability likely | — |
| Lidocaine Hydrochloride 40 mg/mL 63739-0997-64 | McKesson | 1 bottle | $0.222 | AT | Availability likely | — |
| Lidocaine Hydrochloride 40 mg/mL 00116-4025-50 | Xttrium | 1 bottle | $0.222 | AT | Availability likely | — |
| Lidocaine Hydrochloride 40 mg/mL 51672-1411-03 | Sun | 1 bottle | $0.222 | AT | Availability likely | — |
| Lidocaine Hydrochloride 40 mg/mL 83148-0043-50 | The | 1 bottle | $0.222 | AT | Availability likely | — |
| Walgreens Pain Relieving with Turmeric Analgesic 40 mg/mL 00363-1222-01 | Walgreen | 1 bottle | — | — | FDA listed | — |
| Walgreens Pain Relieving with Lavender Analgesic 40 mg/mL 00363-1225-01 | Walgreen | 1 bottle | — | — | FDA listed | — |
| Walgreen Pain Relieving Fragrance Free 4 g/100g 00363-7790-25 | WALGREENS | 1 bottle | — | — | FDA listed | — |
| TopCare Pain Relief Maximum Strength 4 g/100g 36800-0529-25 | TOPCO | 1 bottle | — | — | FDA listed | — |
| Aspercreme with Lidocaine No-Mess Applicator 4 g/100mL 41167-0581-00 | Chattem, | 1 bottle | — | — | FDA listed | — |
| Aspercreme with Lidocaine Essential Oils Rosemary Mint 4 g/100mL 41167-0598-07 | Chattem, | 1 bottle | — | — | FDA listed | — |
| Aspercreme with lidocaine No-Mess Applicator Two Pack 4 g/100mL 41167-0599-09 | Chattem, | 2 bottles | — | — | FDA listed | — |
| Icy Hot Lidocaine No-Mess 4 g/100g 41167-1711-00 | Chattem, | 42.5 g | — | — | FDA listed | — |
| Meijer Odor Free Analgesic Pain Relieving Topical Analgesic 40 mg/mL 41250-0351-01 | Meijer | 1 cylinder | — | — | FDA listed | — |
| Good Sense Pain Relief Roll On 4 g/100g 50804-0187-02 | Geiss, | 71 g | — | — | FDA listed | — |
| Dologesic Roll-On 4 g/100mL 54859-0513-02 | Llorens | 60 ml | — | — | FDA listed | — |
| Theraworx Pain Relief Roll- On- Lidocaine 40 mg/mL 61594-0028-00 | AVADIM | 1 bottle | — | — | FDA listed | — |
| Theraworx Pain Relief Roll-On with Lidocaine for Diabetics 40 mg/mL 61594-0030-00 | AVADIM | 74 ml | — | — | FDA listed | — |
| Theraworx PM Nighttime Maximum Strength Pain Relief 40 mg/mL 61594-0044-00 | AVADIM | 1 bottle | — | — | FDA listed | — |
| Bactine Max Lidocaine Roll-on 2.5oz 4 g/100g 65197-0840-25 | WellSpring | 1 bottle | — | — | FDA listed | — |
| pain relief roll-on 4 g/100mL 69452-0393-63 | Bionpharma | 1 bottle | — | — | FDA listed | — |
| Lipoflavonoid Ear Pain Kids Relief Drops 4 g/100mL 69693-0902-04 | Clarion | 12.4 ml | — | — | FDA listed | — |
| IceQuake Lidocaine Analgesic 4 g/100mL 69822-0430-03 | Southern | 74 ml | — | — | FDA listed | — |
| Lidocaine Pain Relief Roll-On 4 g/100mL 69842-0029-97 | CVS | 1 bottle | — | — | FDA listed | — |
| Leader Lidocaine 4 g/100mL 70000-0099-01 | CARDINAL | 1 bottle | — | — | FDA listed | — |
| Meijer Pain Relieving Max Strength with Lavender Essential Oil Analgesic 40 mg/mL 79481-0019-01 | Meijer | 1 cylinder | — | — | FDA listed | — |
| DOCTORS TOUCH Erase The Pain Lidocaine 40 mg/mLthis 80045-0400-00 | DOCTOR'S | 90 ml | — | — | FDA listed | — |
| Thera Plus Max Strength Lidocaine Pain Relief Liquid 40 mg/mL 80684-0098-00 | Fourstar | 74 ml | — | — | FDA listed | — |
| QUALITY CHOICE Maximum Strength Lidocaine Pain Relief Roll On 4 g/100g 83324-0226-71 | CHAIN | 1 bottle | — | — | FDA listed | — |
| AUVON Pain Relief Roll-on 4 g/100mL 83391-0004-01 | SHENZHEN | 74 ml | — | — | FDA listed | — |
| Lidocaine Hydrochloride 40 mg/mL 76329-6300-05 | International | 25 vials | — | AT | FDA listed | — |
| Lidocaine Hydrochloride 40 mg/mL 51407-0825-50 | Golden | 50 ml | — | AT | FDA listed | — |
| MAXOCAINE Lidocaine Hemp Oil Topical Analgesic 40 mg/mL 72188-0188-00 | Prime | 30 ml | — | — | FDA listed | — |
| equate Maximum Strength Pain Relieving 4% Lidocaine with Lavender Essential Oil Topical analgesic 40 mg/mL 79903-0229-01 | Wal-Mart | 1 bottle | — | — | FDA listed | — |
| Lidocaine Hydrochloride 40 mg/mL 72162-2620-02 | Bryant | 1 bottle | — | AT | FDA listed | — |
| Lidocaine Hydrochloride 40 mg/mL 72162-2627-02 | Bryant | 1 bottle | — | AT | FDA listed | — |
| Lidocaine Hydrochloride 40 mg/mL 10135-0736-51 | Marlex | 1 bottle | — | AT | FDA listed | — |
| Painsil Pain Relief Roll-On 40 mg/mL 87848-0001-00 | Painsil | 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Oct 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2023
On the market since
Apr 2023
📍
2026
Currently FDA-listed
3 years listed
🔓
·
Generic versions listed
see equivalents
✅Generic appears available
FDA-approved generic versions are listed, and recent pricing/market data suggests they may be available — see Therapeutic equivalents.
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.
- FDA Orange Book · refreshed Oct 3, 2026
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 ZY81Z83H0X
Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
-
UNII OZ0E5Y15PZ
A plant extract from arnica flowers, used as a flavoring agent or fragrance component in medicines. It may also provide mild soothing properties to certain topical formulations.
-
UNII 58B69Q84JO
A plant-derived emulsifier made from olive oil and fatty alcohols. It helps blend oil and water ingredients together and stabilizes the product's texture in creams, lotions, and similar 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 9H4PO4Z4FT
A sulfur-containing organic compound used as a solvent and penetration enhancer in medicines. It helps dissolve active ingredients and improve their absorption through skin or mucous membranes.
-
UNII 147D247K3P
Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
-
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 230OU9XXE4
A waxy substance made from glycerin and stearic acid that acts as an emulsifier to blend oily and watery ingredients together. It also helps thicken and stabilize the medicine's texture.
-
UNII 2788Z9758H
A plant extract from licorice root used as a sweetener, flavoring agent, and natural emulsifier in medicines. It helps improve taste and may aid in keeping ingredients evenly mixed throughout the product.
-
UNII BKJ0J3D1BP
A plant-derived ingredient from sunflower flowers, used as a natural colorant and flavoring agent in medicines. It may help provide color or mild taste to the product.
-
UNII 1Q953B4O4F
Ilex paraguariensis leaf, commonly known as yerba mate, is a plant extract used in medicines as a flavoring agent and to add botanical content. It may also contribute mild preservative properties to the formulation.
-
UNII 4PW41QCO2M
Indian frankincense is a natural resin extracted from trees native to India. It is used in medicines as a binder and thickening agent to help hold ingredients together and improve texture.
-
UNII 0RE8K4LNJS
Isopropyl myristate is an oily liquid made from coconut or palm oil. It's used in medicines as an emollient and penetration enhancer to help the medicine absorb through skin or improve spreadability in topical products.
-
UNII ZBP1YXW0H8
A fragrant oil extracted from lavender plants, used as a flavoring and scent agent in medicines to improve taste and aroma.
-
UNII DE08037SAB
Magnesium sulfate is a mineral salt that acts as an osmotic agent in medications. It draws water into the intestines to soften stool or is used as a filler and processing aid in some solid dosage forms.
-
UNII HIE492ZZ3T
Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
-
UNII MDL271E3GR
Sorbitan olivate is an emulsifier derived from sorbitol and olive oil. It helps blend water and oil ingredients together to maintain consistent texture and appearance throughout the medicine.
-
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 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.
20 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesAloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Amica Montana Flower Extract, Boswellia Serrata Extract, Cetearyl Olivate, Cetyl Alcohol, Ethylhexylglycerin, Glycerin, Glyceryl Stearate, Glycyrrhiza Glabra (Licorice) Extract, Helianthus Annuus (Sunflower) Oil, Ilex Paraguariensis (Yerba Mate) Extract, lsopropyl Myristate, Lavandula Angustifolia (Lavender) Oil, Magnesium Sulfate, Methylsulfonylmethane (MSM), Phenoxyethanol, Sorbitan Olivate, Stearic Acid, Tocopheryl Acetate (Vitamin E).
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.- FDA label on DailyMed · label index refreshed Oct 1, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
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
LabelerDOCTOR'S CHOICE MEDICAL, LLC
FDA applicationM015 (OTC MONOGRAPH DRUG)
Labeler code80045
First marketedApr 2023
Product typeHuman Otc Drug
Portfolio3 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 openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
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
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
📄 Do Not Use
📄 When Using This Product
📄 Stop Use and Ask a Doctor If
🤰 If Pregnant or Breast-Feeding
📄 Keep Out of Reach of Children
📄 Questions or Comments
📄 Package Label / Principal Display Panel
🎯 Indications and Usage ▾
Uses: For the temporary relief of pain.
⏱️ Dosage and Administration ▾
Directions: Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: consult a doctor.
⚠️ Warnings ▾
Warnings: not intended for ingestion. For external use only Do not use in large quantities, particularly over raw surfaces, or blistered areas. When using this product Avoid contact with the eyes.
Avoid contact with the eyes. condition worsens, or if 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 a Poison Control Center right away.
If pregnant or breast-feeding, ask a health professional before use
🧪 Active Ingredient ▾
Active Ingredients Lidocaine HCL 4.00 % Purpose Topical Analgesic
🧪 Inactive Ingredients ▾
Inactive ingredients: Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Amica Montana Flower Extract, Boswellia Serrata Extract, Cetearyl Olivate, Cetyl Alcohol, Ethylhexylglycerin, Glycerin, Glyceryl Stearate, Glycyrrhiza Glabra (Licorice) Extract, Helianthus Annuus (Sunflower) Oil, Ilex Paraguariensis (Yerba Mate) Extract, lsopropyl Myristate, Lavandula Angustifolia (Lavender) Oil, Magnesium Sulfate, Methylsulfonylmethane (MSM), Phenoxyethanol, Sorbitan Olivate, Stearic Acid, Tocopheryl Acetate (Vitamin E).
🎯 Purpose ▾
Purpose Topical Analgesic
📄 Do Not Use ▾
Do not use in large quantities, particularly over raw surfaces, or blistered areas.
📄 When Using This Product ▾
When using this product Avoid contact with the eyes.
📄 Stop Use and Ask a Doctor If ▾
Avoid contact with the eyes. condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.
🤰 If Pregnant or Breast-Feeding ▾
If pregnant or breast-feeding, ask a health professional before use
📄 Keep Out of Reach of Children ▾
Keep out of reach of children. If swallowed, get medical help, or contact a Poison Control Center right away.
📄 Questions or Comments ▾
Questions: 954-546-0990
📄 Package Label / Principal Display Panel ▾
Package Labeling: Label
No label section mentions that — try another word, or open the full label on DailyMed below.
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 DOCTORS TOUCH Erase The Pain Lidocaine (this brand).
Top reported reactions
Age at onset
Reporter sex
Male · 35%
Female · 65%
Unknown · 1%
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
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 DOCTOR'S CHOICE MEDICAL, LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
DOCTOR'S CHOICE MEDICAL, 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.
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.