Breatheze

Product NDC
48951-2079
11-digit product format
489512079
Labeler code
48951
Product ID
48951-2079_6a861315-d9c9-4400-e053-2a91aa0aeef7
Type
HUMAN OTC DRUG
Nonproprietary name
Breatheze
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
PAPRIKA; EUPHRASIA STRICTA; LONICERA DASYSTYLA FLOWER BUD; JUJUBE FRUIT; URTICA DIOICA ROOT; URTICA DIOICA LEAF
Active strength
2 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct48951-2079DDiscontinued by firm2026-10-05
excluded packagepackage48951-207948951-2079-3DDiscontinued by firm2026-10-05

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 · 24 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage48951-2079-3d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage48951-2079-3f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31excluded productproduct2ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-31excluded packagepackage48951-2079-32ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28excluded productproducta1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-28excluded packagepackage48951-2079-3a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21excluded productproductcfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-21excluded packagepackage48951-2079-3cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10excluded productproductcdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-10excluded packagepackage48951-2079-3cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31excluded productproduct302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-31excluded packagepackage48951-2079-3302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20excluded productproducted331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-20excluded packagepackage48951-2079-3ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10excluded productproduct0efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage48951-2079-30efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08excluded productproductad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-08excluded packagepackage48951-2079-3ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03excluded productproduct367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-03excluded packagepackage48951-2079-3367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09excluded productproduct557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-09excluded packagepackage48951-2079-3557ba5c1ecfa…9c80585c8c6e…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
EUPHRASIA STRICTAACTIVE INGREDIENTC9642I91WLBREATHEZE LIQUID [URIEL PHARMACY INC.]1
JUJUBE FRUITACTIVE INGREDIENTG55HNL2C70BREATHEZE LIQUID [URIEL PHARMACY INC.]1
LONICERA DASYSTYLA FLOWER BUDACTIVE INGREDIENTJ133K038DYBREATHEZE LIQUID [URIEL PHARMACY INC.]1
PAPRIKAACTIVE INGREDIENTX72Z47861VBREATHEZE LIQUID [URIEL PHARMACY INC.]1
URTICA DIOICA LEAFACTIVE INGREDIENTX6M0DRN46QBREATHEZE LIQUID [URIEL PHARMACY INC.]1
URTICA DIOICA ROOTACTIVE INGREDIENTJ8HE8A6E5TBREATHEZE LIQUID [URIEL PHARMACY INC.]1
EUPHRASIA STRICTAACTIVE MOIETYC9642I91WLBREATHEZE LIQUID [URIEL PHARMACY INC.]1
JUJUBE FRUITACTIVE MOIETYG55HNL2C70BREATHEZE LIQUID [URIEL PHARMACY INC.]1
LONICERA DASYSTYLA FLOWER BUDACTIVE MOIETYJ133K038DYBREATHEZE LIQUID [URIEL PHARMACY INC.]1
PAPRIKAACTIVE MOIETYX72Z47861VBREATHEZE LIQUID [URIEL PHARMACY INC.]1
URTICA DIOICA LEAFACTIVE MOIETYX6M0DRN46QBREATHEZE LIQUID [URIEL PHARMACY INC.]1
URTICA DIOICA ROOTACTIVE MOIETYJ8HE8A6E5TBREATHEZE LIQUID [URIEL PHARMACY INC.]1
GLYCERININACTIVE INGREDIENTPDC6A3C0OXBREATHEZE LIQUID [URIEL PHARMACY INC.]1
LEMONINACTIVE INGREDIENT24RS0A988OBREATHEZE LIQUID [URIEL PHARMACY INC.]1
PROPOLIS WAXINACTIVE INGREDIENT6Y8XYV2NOFBREATHEZE LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RBREATHEZE LIQUID [URIEL PHARMACY INC.]1