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

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 dateDatasetScopePackage NDCCodeStatusSnapshotSource SHA-256
2022-08-30 03:57 UTC · source 2022-08-29excluded productproductIInactivated by FDAfb8cb913e6d1…eb8c232b6be0…
2022-08-30 03:57 UTC · source 2022-08-29excluded packagepackage43406-0626-1IInactivated by FDAfb8cb913e6d1…eb8c232b6be0…
2022-04-09 23:13 UTC · source 2022-04-08excluded productproductIInactivated by FDA86f5da6cb304…a595104c45d7…
2022-04-09 23:13 UTC · source 2022-04-08excluded packagepackage43406-0626-1IInactivated by FDA86f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01excluded productproductIInactivated by FDAbd6a592717d7…303034d00443…
2022-04-04 05:40 UTC · source 2022-04-01excluded packagepackage43406-0626-1IInactivated by FDAbd6a592717d7…303034d00443…
2019-12-08 06:16 UTC · source 2019-12-05excluded productproductEExcluded after deficient or non-compliant submission was not corrected110d247fa046…a55b01930146…
2019-12-08 06:16 UTC · source 2019-12-05excluded packagepackage43406-0626-1EExcluded after deficient or non-compliant submission was not corrected110d247fa046…a55b01930146…

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
OYSTER SHELL CALCIUM CARBONATE, CRUDE30 [hp_X]/mL
LOBELIA INFLATA30 [hp_X]/mL
SODIUM SULFATE30 [hp_C]/mL
SPONGIA OFFICINALIS SKELETON, ROASTED30 [hp_X]/mL
PHOSPHORUS30 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 8 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
01Q9PC255DInternal UNII lookup
DL6OZ476V3Internal UNII lookup
S7V92P67HOInternal UNII lookup
2E32821G6IInternal UNII lookup
9PP1T3TC5UInternal UNII lookup
0YPR65R21JInternal UNII lookup
1PIP394IIDInternal UNII lookup
27YLU75U4WInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
97164607-bc12-44cc-84e8-f2ebc0783bd9Available on FDA.report

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#

Effective, Related label table
EffectiveRelated label
2023-01-10CONGESTION HP
2022-01-28CONGESTION HP
2020-06-02CONGESTION HP
2020-01-31CONGESTION 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

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CONGESTION HPAMMONIUM CHLORIDE, ANTIMONY POTASSIUM TARTRATE, ARSENIC TRIOXIDE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, LOBELIA INFLATA, SODIUM SULFATE, SPONGIA OFFICINALIS SKELETON, ROASTED, PHOSPHORUSNatural Creations, Inc.97164607-bc12-44cc-84e8-f2ebc0783bd92025-11-20WarningsExact identifier
ndc (product): 43406-0626

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