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 149 of 149 · 2,973 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Bio Rock Water ROCK WATER BioActive Nutritional, Inc. 178bd16d-0d4f-49d8-866b-8ab3a3c6889d 2018-07-30 Warnings Exact identifier unii: 059QF0KO0R Ammonia N-13 AMMONIA N-13 Cardinal Health 414, LLC 4c563174-c7cd-4224-b865-4da2f39c21c0 2018-07-11 Warnings, Adverse reactions Exact identifier unii: 9OQO0E343Z Discount Drug Mart Vitamin E Hand Sanitizer ETHYL ALCOHOL Discount Drug Mart 8ce10d80-baab-4647-9abb-ebfd9009a172 2018-02-09 Warnings Exact identifier unii: 3K9958V90M KidzStuff Hand Sanitizer ALCOHOL JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD. 7ecf92e5-0ad6-41f0-bd02-2f79acb2b722 2018-01-17 Warnings Exact identifier unii: 3K9958V90M Isopropyl Alcohol ALCOHOL Zee Medical 8dc593e3-1163-4978-a39c-a9b29074699a 2017-12-11 Warnings Exact identifier unii: 3K9958V90M Sterile Water WATER Baxter Healthcare Corporation ef3e79c5-3f58-4b36-a296-64b7d9a651c1 2017-10-17 Warnings, Adverse reactions Exact identifier unii: 059QF0KO0R Alcohol Wipes ALCOHOL JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD. 14dbe9dc-2504-4181-9565-5fa7c1a9c377 2017-10-09 Warnings Exact identifier unii: 3K9958V90M Freeman Packaging Hand Sanitizer ALCOHOL JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD. 9827418a-3ab6-447b-8f8a-9eacb56d3a89 2017-10-09 Warnings Exact identifier unii: 3K9958V90M ONID Wipe ETHANOL ONID Technology Corp 83d8b8b6-6257-4553-9441-901bb02c3d60 2017-06-28 Exact identifier unii: 3K9958V90M Eye Wash WATER CVS Pharmacy 049cee29-7ec2-4d5b-8308-f522acde43a7 2017-03-29 Warnings Exact identifier unii: 059QF0KO0R Sterile Water WATER Baxter Healthcare Company 210dc9ab-d6ca-4552-ac19-1be17792d290 2016-05-31 Warnings, Adverse reactions Exact identifier unii: 059QF0KO0R CVS Hand Sanitizer ALCOHOL CVS d0081c50-c0d2-436a-ba83-5d1982ae64b7 2015-08-17 Warnings Exact identifier unii: 3K9958V90M Instant Hand Sanitizer ALCOHOL Safetec of America, Inc. f9e30645-491b-4f54-acfd-f863ee235607 2013-08-07 Warnings Exact identifier unii: 3K9958V90M
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.