Home › NDC Lookup › Ingredients › Neomycin Sulfate, Polymyxin B Sulfate, A... › 11673-0770-14
Antibiotic and Pain Relief neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride 10000 [USP'U]/g; 3.5 mg/g; 10 mg/g Cream — NDC 11673-0770-14 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Antibiotic and Pain Relief neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride 10000 [USP'U]/g; 3.5 mg/g; 10 mg/g Cream — NDC 11673-770-14 (Billing 11673-0770-14)

by Target Corporation · 1 TUBE in 1 CARTON / 14 g in 1 TUBE

This is a package of Antibiotic and Pain Relief neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride 10000 [USP'U]/g; 3.5 mg/g; 10 mg/g Cream from Target Corporation, marketed since Jan 2024 and currently FDA-listed. It is this product's only package size.

NDC 11673-0770-14
🏷️ FDA NDC (as labeled) 11673-770-14 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 11673-770-14 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
11673 labeler · 770 product · 14 package
Package marketed since
Jan 31, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0732953852008
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 11673-770-14
Product NDC 11673-770
11-digit billing NDC 11673077014
RxCUI 1359360
UNII 19371312D4, 057Y626693, 88AYB867L5
UPC 0732953852008
Application # M004
SPL Set ID 050be94c-1fbb-4d84-82c6-841aac8f318e
Established class (EPC) Aminoglycoside Antibacterial; Polymyxin-class Antibacterial
Chemical class Aminoglycosides; Polymyxins
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-01-31
Route TOPICAL
Dosage form CREAM
Substance POLYMYXIN B SULFATE; NEOMYCIN SULFATE; PRAMOXINE HYDROCHLORIDE

Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification

GPI-14 62100010002810
GPI class TGT Nicotine
Quick answers
  • GPI-14 (Medi-Span): 62100010002810
  • RxCUI (RxNorm): 1359360
Why two NDCs? The FDA registers this code as 11673-770-14 — 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 → 11673-0770-14. 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 Local anesthetics class.

Drug family (ATC) 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.

Clinical

🧪 What is this product?

This is a topical antibiotic and pain relief cream marketed as an over-the-counter monograph drug. It contains neomycin sulfate and polymyxin b sulfate, which are antibiotics typically used to help prevent or treat bacterial skin infections in minor cuts and scrapes. The cream also contains pramoxine hydrochloride, a local anesthetic commonly used to numb minor pain and itching on the skin. This combination product is meant for external use only on 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 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.
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
11673-0770-14 You're viewing this Main listing 1 TUBE in 1 CARTON / 14 g in 1 TUBE 2024-01-31 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Good Neighbor Pharmacy Antibiotic and Pain Relief 3.5 mg/g; 10 mg/g; 10000 [USP'U]/g 46122-0244-03 Amerisource 1 tube $0.097 — Availability likely —
Antibiotic and Pain Relief 3.5 mg/g; 10000 [USP'U]/g; 10 mg/g 70677-1218-01 STRATEGIC 1 tube $0.189 — Availability likely —
Walgreens Kids Multi-Antibiotic with Pain Relief Cream 10000 [USP'U]/g; 3.5 mg/g; 10 mg/g 00363-2122-14 Walgreens 1 tube — — FDA listed —
Walgreens Multi-Antibiotic with Pain Relief Cream 10000 [USP'U]/g; 3.5 mg/g; 10 mg/g 00363-2123-14 Walgreens 1 tube — — FDA listed —
Antibiotic Plus Pain Relief 3.5 mg/g; 10000 [iU]/g; 10 mg/g 11673-0393-01 TARGET 1 tube — — FDA listed —
Antibiotic and Pain Relief 10000 [USP'U]/g; 3.5 mg/g; 10 mg/gthis 11673-0770-14 Target 1 tube — — FDA listed —
Signature Care First Aid Antibiotic 3.5 mg/g; 10 mg/g; 10000 [USP'U]/g 21130-0559-58 Safeway 1 tube — — FDA listed —
antibiotic plus pain relief 3.5 mg/g; 10 mg/g; 10000 [USP'U]/g 30142-0790-58 Kroger 1 tube — — FDA listed —
TopCare Antibiotic Plus Pain Relief 3.5 mg/g; 10000 [iU]/g; 10 mg/g 36800-0381-01 Topco 1 tube — — FDA listed —
Topcare Antibiotic 3.5 mg/g; 10000 [USP'U]/g; 10 mg/g 36800-0976-58 Topco 1 tube — — FDA listed —
antibiotic 3.5 mg/g; 10 mg/g; 10000 [USP'U]/g 37808-0005-58 H 1 tube — — FDA listed —
Publix antibiotic plus Pain Relief 3.5 mg/g; 10000 [iU]/g; 10 mg/g 41415-0076-75 Publix 1 tube — — FDA listed —
Equate Antibiotic Plus Pain Relief 3.5 mg/g; 10000 [USP'U]/g; 10 mg/g 49035-0847-05 WalMart 1 tube — — FDA listed —
DG Health Antibiotic 3.5 mg/g; 10 mg/g; 10000 [USP'U]/g 55910-0061-64 Dolgencorp 1 tube — — FDA listed —
Family Care Antibiotic Pain Relief 0.33oz 10 mg/g; 10000 [USP'U]/g; 3.5 mg/g 65923-0578-33 United 1 tube — — FDA listed —
Premier Value Max Strength Antibiotic plus pain relief 3.5 mg/g; 10 mg/g; 10000 [USP'U]/g 68016-0296-05 Pharmacy 1 tube — — FDA listed —
Dual Action Cream 3.5 mg/g; 10 mg/g; 10000 [USP'U]/g 69396-0071-01 Trifecta 1 tube — — FDA listed —
Antibiotic and Pain Relief 3.5 mg/g; 10 mg/g; 10000 [USP'U]/g 69842-0754-58 CVS 1 tube — — FDA listed —
Neosporin Kids Plus Pain Relief 3.5 mg/g; 10000 [iU]/g; 10 mg/g 69968-0054-01 Kenvue 1 tube — — FDA listed —
Neosporin Plus Pain Relief First Aid Antibiotic/Pain Relieving 3.5 mg/g; 10000 [USP'U]/g; 10 mg/g 69968-0055-01 Kenvue 1 tube — — FDA listed —
first aid antibiotic and pain relief 3.5 mg/g; 10 mg/g; 10000 [USP'U]/g 79481-0809-00 Meijer, 1 tube — — 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

🏛️
2024
On the market since
Jan 2024
📍
2026
Currently FDA-listed
2 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 2DMT128M1S
    A waxy solid derived from plant or animal sources. It acts as an emulsifier to blend oil and water components, and also thickens the medicine to give it the right texture and consistency.
  • UNII FCZ5MH785I
    A waxy substance made from glycerin and stearic acid. It works as an emulsifier to help mix oil and water ingredients together, and as a thickener to give the medicine its proper texture and consistency.
  • UNII A2I8C7HI9T
    Methylparaben is a preservative derived from benzoic acid that prevents growth of bacteria, fungi, and mold in medicines. It extends the product's shelf life and maintains safety during storage.
  • UNII T5L8T28FGP
    Mineral oil is a clear, odorless liquid derived from crude oil. It acts as a lubricant and emollient in medications, helping pills slide smoothly during manufacturing and aiding moisture retention in topical products.
  • 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 E4GA8884NN
    Phosphoric acid is a weak mineral acid used in medicines as a buffer and pH adjuster. It helps stabilize the product and control its acidity level.
  • UNII YRC528SWUY
    A waxy emulsifier made from plant-derived fatty alcohols. It helps blend oil and water-based ingredients together and improves how the medicine spreads and absorbs.
  • 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.

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

The official label also statesCeteareth-20, Cetearyl Alcohol, Glyceryl Stearate SE, Methylparaben, Mineral Oil, Phosphoric Acid, Propylene Glycol, Purified Water, White Petrolatum

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

LabelerTarget Corporation
FDA applicationM004 (OTC MONOGRAPH DRUG)
Labeler code11673
First marketedJan 2024
Product typeHuman Otc Drug
Portfolio409 products on file

More NDCs from Target Corporation labeler code 11673

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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 20 words ▾

Uses first aid to prevent infection and for the temporary relief of pain or discomfort in minor: cuts scapes burns

⏱️ Dosage and Administration 32 words ▾

Directions clean the affected area apply a small amount (equal to surface area of tip of finger) on the area 1 to 3 times daily. may be covered with a sterile bandage

⚠️ Warnings 86 words ▾

Warnings For external use only Allergy alert do not use if you are allergic to any of the ingredients Do not use in or near the eyes or on large areas of the body Ask a doctor before use if you have deep or puncture wounds animal bites serious burns Stop use and ask a doctor if condition persists or gets worse symptoms last for more than 7 days or clear up and come back within a few days a rash or other allergic reaction develops

🧪 Active Ingredient 14 words ▾

Active ingredients Neomycin Sulfate (3.5mg) Polymixin B Sulfate (10,000 units) Pramoxine Hydrochloride (10 mg)

🧪 Inactive Ingredients 19 words ▾

Inactive ingredients Ceteareth-20, Cetearyl Alcohol, Glyceryl Stearate SE, Methylparaben, Mineral Oil, Phosphoric Acid, Propylene Glycol, Purified Water, White Petrolatum

🎯 Purpose 9 words ▾

Purpose First Aid Antibiotic First Aid Antibiotic External Analgesic

📄 Keep Out of Reach of Children 19 words ▾

Keep out of the reach of children. If swallowed get medical help or contact a Poison Control Center immediately.

📄 Other Information 10 words ▾

Other inofrmation Store at a controlled room temperature 68º-77ºF (20º-25ºC)

📄 Questions or Comments 4 words ▾

Questions or comment? 1-800-910-6874

📄 Package Label / Principal Display Panel 30 words ▾

Principal Display Panel Target up&Up NDC 11673-770-14 Maximum Strength Pain Releiving & Infection Protection Neomycin Sulfate/ Polymyxin B Sulfate / Pramoxine HCL NET WT 0.5oz (14g) 291010 Tube 591010 Carton

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 Neomycin, polymyxin B, pramoxine hydrochloride — the ingredient across all brands.

Top reported reactions

Drug Hypersensitivity7
Constipation6
Rash6
Fatigue5
Pain5
Urinary Tract Infection5
Decreased Appetite4

Age at onset

Adult8
Elderly3

Reporter sex

68 reports
Male · 38%
Female · 62%

Serious outcomes

Hospitalization18
Life-threatening2
Death2
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 8 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 Target Corporation. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Target Corporation 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.
← 11673-0769-14 · TARGET 11673-0771-01 · Target →
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.