Home NDC 71491-100 Viabecline
Product NDC 71491-100
11-digit product format 714910100
Labeler code 71491
Product ID 71491-100_0b6dc9f9-4456-e765-e063-6394a90ac6c8
Type HUMAN OTC DRUG
Nonproprietary name TETRACYCLINE HYDROCHLORIDE
Dosage form OINTMENT
Route TOPICAL
Labeler Accuria, LLC
Application M004
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-06-14
Substance TETRACYCLINE HYDROCHLORIDE
Active strength 30 mg/mL
Pharmacologic classes Tetracycline-class Antimicrobial [EPC], Tetracyclines [CS]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Viabecline
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TETRACYCLINE HYDROCHLORIDE 30 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination P6R62377KV Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1542813 Internal RxNorm lookup 1926470 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71491-100-00 Viabecline 5 mL in 1 BOTTLE, DROPPER OINTMENT 5 4 71491-100-01 Viabecline 15 mL in 1 BOTTLE, DROPPER OINTMENT 15 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71491-100 VIABECLINE (TETRACYCLINE HYDROCHLORIDE) OINTMENT [ACCURIA, LLC] 4 Current NDC, Legacy NDC, 2 package rows 20231202_9fd7041a-6c23-4332-90fe-759bb4aea2ae.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 22 of 22 · 424 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Family Wellness Antiseptic and Pain Relief BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HYDROCHLORIDE FRONT PHARMACEUTICAL PLC cb7fdcde-2bd8-4834-ba4e-4d6fd1512599 2023-10-26 Warnings Exact identifier application number: M004 GENUINE FIRST AID Antibiotic BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE Nantong Health & Beyond Hygienic Products Inc. 23abfe12-5b50-4b49-878e-4fcdb6c341fd 2023-10-19 Warnings Exact identifier application number: M004 EVERLIT CARE Triple Antibiotic BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE Nantong Health & Beyond Hygienic Products Inc. f4921508-c32f-426f-a2f0-16c3acbd4713 2023-10-14 Warnings Exact identifier application number: M004 Cuadriderma BACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE ProMex LLC 4fa99b96-ab4b-4523-82bc-343dbaf39fb6 2022-01-25 Warnings Exact identifier application number: M004
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71491-100-00 71491010000 5 mL in 1 BOTTLE, DROPPER (71491-100-00) 5 ml 2017-06-15 0000-00-00 No No Current 71491-100-01 71491010001 15 mL in 1 BOTTLE, DROPPER (71491-100-01) 15 ml 2017-06-15 0000-00-00 No No Current