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

Additional Listing Data#

Finished product
Yes
Brand name base
Household Antigens

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACETONE9 [hp_X]/mL
AMMONIUM CHLORIDE9 [hp_X]/mL
ANEMONE PRATENSIS12 [hp_X]/mL
BENZENE9 [hp_X]/mL
BISPHENOL A9 [hp_X]/mL
BUTYL ACETATE9 [hp_X]/mL
ETHYL ACETATE9 [hp_X]/mL
GRAPHITE12 [hp_X]/mL
KEROSENE9 [hp_X]/mL
NITRIC ACID12 [hp_X]/mL
PROPYLENE GLYCOL9 [hp_X]/mL
SEMECARPUS ANACARDIUM JUICE12 [hp_X]/mL
SODIUM LAURYL SULFATE9 [hp_X]/mL
SODIUM TRIPOLYPHOSPHATE9 [hp_X]/mL
SULFUR12 [hp_X]/mL
TOLUENE9 [hp_X]/mL
TURPENTINE OIL9 [hp_X]/mL
XYLENE (MIXED ISOMERS)9 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii1364PS73AF, 01Q9PC255D, 8E272251DI, J64922108F, MLT3645I99, 464P5N1905, 76845O8NMZ, 4QQN74LH4O, 1C89KKC04E, 411VRN1TV4, 6DC9Q167V3, Y0F0BU8RDU, 368GB5141J, 5HK03SA80J, 70FD1KFU70, 3FPU23BG52, C5H0QJ6V7F, D856J1047R

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0536-12024-09-27C16284748780-1f386c64a-0001-0266-e053-dadaa90a7c1aDrugs:
44911-0536-12023-01-30C16284748780-1f386c64a-0001-0266-e053-dadaa90a7c1aDrugs:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0536-1Household Antigens30 mL in 1 BOTTLE, DROPPERLIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0536HOUSEHOLD 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.]3Current NDC, Legacy NDC, 1 package rows20240929_87c92497-8a51-4977-87fe-e0b4c6bafb19.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
44911-0536-14491105360130 mL in 1 BOTTLE, DROPPER (44911-0536-1) 30 ml2020-03-102028-05-17NoNoCurrent