Home NDC 44911-0536 Household Antigens
Product NDC 44911-0536
11-digit product format 449110536
Labeler code 44911
Product ID 44911-0536_3cc00ed9-9470-439d-ba3c-7f367bda7bc6
Type HUMAN OTC DRUG
Nonproprietary name Acetone, Sodium Tripolyphosphate, Propylene Glycol, Benzinum, Ammonium Muriaticum, Sodium Lauryl Sulfate, Terebinthina, Butyl Acetate, Ethyl Acetate, Toluene, Xylene, Bisphenol A, Petroleum, Anacardium Orientale, Graphites, Nitricum Acidum, Pulsatilla (Pratensis), Sulphur
Dosage form LIQUID
Route ORAL
Labeler Energique, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2020-03-10
Marketing end 2028-05-17
Substance ACETONE; AMMONIUM CHLORIDE; ANEMONE PRATENSIS; BENZENE; BISPHENOL A; BUTYL ACETATE; ETHYL ACETATE; GRAPHITE; KEROSENE; NITRIC ACID; PROPYLENE GLYCOL; SEMECARPUS ANACARDIUM JUICE; SODIUM LAURYL SULFATE; SODIUM TRIPOLYPHOSPHATE; SULFUR; TOLUENE; TURPENTINE OIL; XYLENE (MIXED ISOMERS)
Active strength 9; 9; 12; 9; 9; 9; 9; 12; 9; 12; 9; 12; 9; 9; 12; 9; 9; 9 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag No
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 8 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 44911-0536-1 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 44911-0536-1 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 44911-0536-1 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 44911-0536-1 1332a3947898…d4bfe170f9cd…
Additional Listing Data#
Finished product Yes
Brand name base Household Antigens Active Ingredients# Ingredient, Strength table Ingredient Strength ACETONE 9 [hp_X]/mL SODIUM TRIPOLYPHOSPHATE 9 [hp_X]/mL PROPYLENE GLYCOL 12 [hp_X]/mL BENZENE 9 [hp_X]/mL AMMONIUM CHLORIDE 9 [hp_X]/mL SODIUM LAURYL SULFATE 9 [hp_X]/mL TURPENTINE OIL 9 [hp_X]/mL BUTYL ACETATE 12 [hp_X]/mL ETHYL ACETATE 9 [hp_X]/mL TOLUENE 12 [hp_X]/mL XYLENE (MIXED ISOMERS) 9 [hp_X]/mL BISPHENOL A 12 [hp_X]/mL KEROSENE 9 [hp_X]/mL SEMECARPUS ANACARDIUM JUICE 9 [hp_X]/mL GRAPHITE 12 [hp_X]/mL NITRIC ACID 9 [hp_X]/mL ANEMONE PRATENSIS 9 [hp_X]/mL SULFUR 9 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 18 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 44911-0536-1 Household Antigens 30 mL in 1 BOTTLE, DROPPER LIQUID 30 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 44911-0536 HOUSEHOLD ANTIGENS (ACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, BUTYL ACETATE, ETHYL ACETATE, TOLUENE, XYLENE, BISPHENOL A, PETROLEUM, ANACARDIUM ORIENTALE, GRAPHITES, NITRICUM ACIDUM, PULSATILLA (PRATENSIS), SULPHUR) LIQUID [ENERGIQUE, INC.] 3 Current NDC, Legacy NDC, 1 package rows 20240929_87c92497-8a51-4977-87fe-e0b4c6bafb19.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 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Household Antigens ACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, BUTYL ACETATE, ETHYL ACETATE, TOLUENE, XYLENE, BISPHENOL A, PETROLEUM, ANACARDIUM ORIENTALE, GRAPHITES, NITRICUM ACIDUM, PULSATILLA (PRATENSIS), SULPHUR Energique, Inc. 87c92497-8a51-4977-87fe-e0b4c6bafb19 2024-09-27 Warnings Exact identifier ndc (product): 44911-0536
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 44911-0536-1 44911053601 30 mL in 1 BOTTLE, DROPPER (44911-0536-1) 30 ml 2020-03-10 2028-05-17 No No Current