FDA.reportPublic FDA data

CONGESTION HP

Product NDC
43406-0626
11-digit product format
434060626
Labeler code
43406
Product ID
43406-0626_b8743338-e002-4fb1-8bc1-27bbbf066102
Type
HUMAN OTC DRUG
Nonproprietary name
Ammonium Chloride, Antimony Potassium Tartrate, Arsenic Trioxide, Oyster Shell Calcium Carbonate, Crude, Lobelia Inflata, Sodium Sulfate, Spongia Officinalis Skeleton, Roasted, Phosphorus
Dosage form
LIQUID
Route
ORAL
Labeler
Natural Creations, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2016-06-01
Substance
AMMONIUM CHLORIDE; ANTIMONY POTASSIUM TARTRATE; ARSENIC TRIOXIDE; LOBELIA INFLATA; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHOSPHORUS; SODIUM SULFATE; SPONGIA OFFICINALIS SKELETON, ROASTED
Active strength
30; 30; 30; 30; 30; 30; 30; 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
CONGESTION HP
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AMMONIUM CHLORIDE30 [hp_X]/mL
ANTIMONY POTASSIUM TARTRATE30 [hp_X]/mL
ARSENIC TRIOXIDE30 [hp_X]/mL
LOBELIA INFLATA30 [hp_X]/mL
OYSTER SHELL CALCIUM CARBONATE, CRUDE30 [hp_X]/mL
PHOSPHORUS30 [hp_C]/mL
SODIUM SULFATE30 [hp_X]/mL
SPONGIA OFFICINALIS SKELETON, ROASTED30 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii01Q9PC255D, DL6OZ476V3, S7V92P67HO, 9PP1T3TC5U, 2E32821G6I, 27YLU75U4W, 0YPR65R21J, 1PIP394IID

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43406-0626-12023-01-10C16284748780-19d75b9d0-1651-f424-e053-dadaa90a57ceCONGESTION HP
43406-0626-12022-01-28C16284748780-19d75b9d0-1651-f424-e053-dadaa90a57ceCONGESTION HP
43406-0626-12020-06-02C16284748780-19d75b9d0-1651-f424-e053-dadaa90a57ceCONGESTION HP
43406-0626-12020-01-31C16284748780-19d75b9d0-1651-f424-e053-dadaa90a57ceCONGESTION HP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43406-0626-1CONGESTION HP30 mL in 1 BOTTLE, DROPPERLIQUID304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43406-0626CONGESTION HP (AMMONIUM CHLORIDE, ANTIMONY POTASSIUM TARTRATE, ARSENIC TRIOXIDE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, LOBELIA INFLATA, SODIUM SULFATE, SPONGIA OFFICINALIS SKELETON, ROASTED, PHOSPHORUS) LIQUID [NATURAL CREATIONS, INC.]3Current NDC, Legacy NDC, 1 package rows20230111_97164607-bc12-44cc-84e8-f2ebc0783bd9.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43406-0626-14340606260130 mL in 1 BOTTLE, DROPPER (43406-0626-1) 30 ml2016-06-010000-00-00NoNoCurrent