antibiotic and pain relief

Generic: neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride

Labeler: target corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name antibiotic and pain relief
Generic Name neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride
Labeler target corporation
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

neomycin sulfate 3.5 mg/g, polymyxin b sulfate 10000 [USP'U]/g, pramoxine hydrochloride 10 mg/g

Manufacturer
Target Corporation

Identifiers & Regulatory

Product NDC 11673-770
Product ID 11673-770_198a8cc8-c708-42c9-b533-0b688475411e
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M004
Listing Expiration 2026-12-31
Marketing Start 2024-01-31

Pharmacologic Class

Classes
aminoglycoside antibacterial [epc] aminoglycosides [cs] polymyxin-class antibacterial [epc] polymyxins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673770
Hyphenated Format 11673-770

Supplemental Identifiers

RxCUI
1359360
UPC
0732953852008
UNII
057Y626693 19371312D4 88AYB867L5

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name antibiotic and pain relief (source: ndc)
Generic Name neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride (source: ndc)
Application Number M004 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 3.5 mg/g
  • 10000 [USP'U]/g
  • 10 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (11673-770-14) / 14 g in 1 TUBE
source: ndc

Packages (1)

11673-770-14 1 TUBE in 1 CARTON (11673-770-14) / 14 g in 1 TUBE

Ingredients (3)

neomycin sulfate (3.5 mg/g) polymyxin b sulfate (10000 [USP'U]/g) pramoxine hydrochloride (10 mg/g)

Linked Drug Pages (1)

Antibiotic and Pain Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "198a8cc8-c708-42c9-b533-0b688475411e", "openfda": {"upc": ["0732953852008"], "unii": ["057Y626693", "19371312D4", "88AYB867L5"], "rxcui": ["1359360"], "spl_set_id": ["050be94c-1fbb-4d84-82c6-841aac8f318e"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (11673-770-14)  / 14 g in 1 TUBE", "package_ndc": "11673-770-14", "marketing_start_date": "20240131"}], "brand_name": "Antibiotic and Pain Relief", "product_id": "11673-770_198a8cc8-c708-42c9-b533-0b688475411e", "dosage_form": "CREAM", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]", "Polymyxin-class Antibacterial [EPC]", "Polymyxins [CS]"], "product_ndc": "11673-770", "generic_name": "neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Antibiotic and Pain Relief", "active_ingredients": [{"name": "NEOMYCIN SULFATE", "strength": "3.5 mg/g"}, {"name": "POLYMYXIN B SULFATE", "strength": "10000 [USP'U]/g"}, {"name": "PRAMOXINE HYDROCHLORIDE", "strength": "10 mg/g"}], "application_number": "M004", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240131", "listing_expiration_date": "20261231"}