Home NDC 55756-133 NDC 55756-133 - Hoofbath Booster HFB50 This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 55756-133
Package NDCs from labels 55756-133-02, 55756-133-01
Manufacturer DeLaval | WestAgro, Inc. | K Klean dba WestAgro, Inc.
Effective date 2022-01-04
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type DeLaval Hoofbath Booster HFB50 DeLaval | WestAgro, Inc. | K Klean dba WestAgro, Inc. 2022-01-04 OTC ANIMAL DRUG LABEL
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded HYDROCHLORIC ACID ACTIVE INGREDIENT QTT17582CB HOOFBATH BOOSTER HFB50 (HYDROCHLORIC ACID) SOLUTION, CONCENTRATE [DELAVAL] 2 HYDROCHLORIC ACID ACTIVE MOIETY QTT17582CB HOOFBATH BOOSTER HFB50 (HYDROCHLORIC ACID) SOLUTION, CONCENTRATE [DELAVAL] 2 ALCOHOL INACTIVE INGREDIENT 3K9958V90M HOOFBATH BOOSTER HFB50 (HYDROCHLORIC ACID) SOLUTION, CONCENTRATE [DELAVAL] 2 AMMONIA N-13 INACTIVE INGREDIENT 9OQO0E343Z HOOFBATH BOOSTER HFB50 (HYDROCHLORIC ACID) SOLUTION, CONCENTRATE [DELAVAL] 2 DIDECYLDIMETHYLAMMONIUM CHLORIDE INACTIVE INGREDIENT JXN40O9Y9B HOOFBATH BOOSTER HFB50 (HYDROCHLORIC ACID) SOLUTION, CONCENTRATE [DELAVAL] 2 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA HOOFBATH BOOSTER HFB50 (HYDROCHLORIC ACID) SOLUTION, CONCENTRATE [DELAVAL] 2 N-ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C18) INACTIVE INGREDIENT 9U1Q4T4ZYS HOOFBATH BOOSTER HFB50 (HYDROCHLORIC ACID) SOLUTION, CONCENTRATE [DELAVAL] 2 WATER INACTIVE INGREDIENT 059QF0KO0R HOOFBATH BOOSTER HFB50 (HYDROCHLORIC ACID) SOLUTION, CONCENTRATE [DELAVAL] 2
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 63 of 151 · 3,001 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Retail Hand Sanitizer ALCOHOL Ecolab Inc. 55e65545-9869-413b-8239-bd2d43fe36d8 2025-12-30 Warnings Exact identifier unii: 3K9958V90M MG DermaGel 62 ETHYL ALCOHOL Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc. e6b2cc57-11a6-4808-a30f-8118a8de9fc6 2025-12-29 Warnings Exact identifier unii: 3K9958V90M Refreshify Antiseptic Hand Wipes ALCOHOL Emes Commerce Group Inc. 46d2f10e-e1c2-3ca2-e063-6394a90a602d 2025-12-29 Warnings Exact identifier unii: 3K9958V90M Hand Sanitizer ALCOHOL HAIAN KANGRUI TEXTILE CO., LTD. 4711fb91-8afd-e5db-e063-6394a90a4b9e 2025-12-29 Warnings Exact identifier unii: 3K9958V90M SnugZ Hand Sanitizing Spry HAND SANITIZER SPRAY SnugZ/USA, LLC 9391bc26-57e6-daec-e053-2995a90a1eb6 2025-12-29 Warnings Exact identifier unii: 3K9958V90M SnugZ Beaded Hand Sanitizer Gel BEADED HAND SANITIZER GEL SnugZ/USA, LLC 6deb1142-dfba-a72b-e053-2991aa0aba43 2025-12-29 Warnings Exact identifier unii: 3K9958V90M SnugZ Hand Sanitizing Wipes HAND SANITIZING WIPES SnugZ/USA, LLC c5d9122a-2c67-2387-e053-2a95a90a2c3a 2025-12-29 Warnings Exact identifier unii: 3K9958V90M SnugZ Hand Sanitizer Gel HAND SANITIZER GEL SnugZ/USA, LLC 69bc7a80-0898-4c08-e053-2a91aa0a87a9 2025-12-29 Warnings Exact identifier unii: 3K9958V90M OCUFRESH WATER Optics Laboratory Inc. b8e477a9-66b9-496b-92fb-3d4bbd7b36b5 2025-12-29 Warnings Exact identifier unii: 059QF0KO0R Dehydrated Alcohol ALCOHOL Ajenat Pharmaceuticals LLC 636d6421-cadf-42b3-a431-ba40c06e36d2 2025-12-29 Warnings, Adverse reactions Exact identifier unii: 3K9958V90M Kollourion Eyesalve Eyewash PURIFIED WATER 98.3% Miracle Eye Pharmaceuticals b56d2ab9-169b-b490-e053-2a95a90a80b3 2025-12-28 Warnings Exact identifier unii: 059QF0KO0R Freshnap Plus - 80% Ethyl Alcohol Towelette ALCOHOL TOWELETTE KARI-OUT LLC f4ae66e3-323b-5e2e-e053-2995a90acf42 2025-12-27 Warnings Exact identifier unii: 3K9958V90M FRESH FEELS HAND SANITIZER MIST PISTACHIO MATCHA SCENT ETHYL ALCOHOL Amber Glow Cosmetics Limited dfd59d2e-9036-486a-b25b-7e5fe23421ce 2025-12-26 Warnings Exact identifier unii: 3K9958V90M Hand Sanitizer Gel ETHANOL Zep Inc. c72cf71f-e639-2854-e053-2a95a90ab30e 2025-12-26 Warnings Exact identifier unii: 3K9958V90M Zep Handstand Instant Hand Sanitizer ETHYL ALCOHOL Zep Inc. 9984beca-a66a-785c-e053-2995a90ae5ba 2025-12-26 Warnings Exact identifier unii: 3K9958V90M Zep Hand Sanitizer Wipes ETHANOL Zep Inc. 99867fc5-820e-6d6b-e053-2a95a90a0793 2025-12-26 Warnings Exact identifier unii: 3K9958V90M Ammonia N 13 AMMONIA N-13 Mayo Clinic af70d0da-1c2d-44e4-b4cd-7cce6636c7b9 2025-12-26 Warnings, Adverse reactions Exact identifier unii: 9OQO0E343Z StellaLife Hand Sanitizer ALCOHOL StellaLife, Inc. a65b338d-5019-0cfc-e053-2a95a90ae8b2 2025-12-26 Warnings Exact identifier unii: 3K9958V90M FRESH FEELS HAND SANITIZER MIST PINEAPPLE SUNDAE SCENT ETHYL ALCOHOL Amber Glow Cosmetics Limited ddda3587-1967-474a-8d9b-c6dad5448b2c 2025-12-26 Warnings Exact identifier unii: 3K9958V90M FRESH FEELS HAND SANITIZER MIST BERRY KISS SCENT ETHYL ALCOHOL Amber Glow Cosmetics Limited 39c8767d-46e8-4b26-be52-e5ed7d090d3e 2025-12-26 Warnings Exact identifier unii: 3K9958V90M
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.