triple antibiotic plus pain relief maximum strength
Generic: bacitracin zinc, neomycin sulfate, polymyxin b sulfate and pramoxine hydrochloride
Labeler: chain drug consortium, llcDrug Facts
Product Profile
Brand Name
triple antibiotic plus pain relief maximum strength
Generic Name
bacitracin zinc, neomycin sulfate, polymyxin b sulfate and pramoxine hydrochloride
Labeler
chain drug consortium, llc
Dosage Form
OINTMENT
Routes
Active Ingredients
bacitracin zinc 500 [USP'U]/g, neomycin sulfate 3.5 mg/g, polymyxin b sulfate 10000 [USP'U]/g, pramoxine hydrochloride 10 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
68016-715
Product ID
68016-715_c6bc1e43-7d2c-460d-9465-b17efe3c50ad
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M004
Marketing Start
2015-07-10
Marketing End
2026-12-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68016715
Hyphenated Format
68016-715
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
triple antibiotic plus pain relief maximum strength (source: ndc)
Generic Name
bacitracin zinc, neomycin sulfate, polymyxin b sulfate and pramoxine hydrochloride (source: ndc)
Application Number
M004 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 [USP'U]/g
- 3.5 mg/g
- 10000 [USP'U]/g
- 10 mg/g
Packaging
- 1 TUBE in 1 CARTON (68016-715-01) / 28 g in 1 TUBE
Packages (1)
Ingredients (4)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "c6bc1e43-7d2c-460d-9465-b17efe3c50ad", "openfda": {"upc": ["0840986032424"], "unii": ["89Y4M234ES", "057Y626693", "19371312D4", "88AYB867L5"], "rxcui": ["1359350"], "spl_set_id": ["55ef2205-aaf1-4aa4-917f-2b4cfa43b77e"], "manufacturer_name": ["Chain Drug Consortium, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (68016-715-01) / 28 g in 1 TUBE", "package_ndc": "68016-715-01", "marketing_end_date": "20261231", "marketing_start_date": "20150710"}], "brand_name": "Triple Antibiotic plus Pain Relief Maximum Strength", "product_id": "68016-715_c6bc1e43-7d2c-460d-9465-b17efe3c50ad", "dosage_form": "OINTMENT", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]", "Decreased Cell Wall Synthesis & Repair [PE]", "Polymyxin-class Antibacterial [EPC]", "Polymyxins [CS]"], "product_ndc": "68016-715", "generic_name": "bacitracin zinc, neomycin sulfate, polymyxin b sulfate and pramoxine hydrochloride", "labeler_name": "Chain Drug Consortium, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Triple Antibiotic plus Pain Relief", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "BACITRACIN ZINC", "strength": "500 [USP'U]/g"}, {"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_end_date": "20261231", "marketing_start_date": "20150710"}