ENT Support

Product NDC

43742-1119

11-digit product format

437421119

Labeler code

43742

Product ID

43742-1119_d2ba8c90-9e56-45ce-bbd4-032c0e10b4ab

Type

HUMAN OTC DRUG

Nonproprietary name

Pulsatilla (Vulgaris), Euphorbium Officinarum, Luffa Operculata, Mercurius Iodatus Ruber, Argentum Nitricum, Hepar Sulphuris Calcareum, Influenzinum (2017-2018), Sinusitisinum, Aspergillus Niger, Candida Albicans, Gallicum Acidum, Mucor Racemosus, Mutabile Bacillus (Bach)

Dosage form

LIQUID

Route

ORAL

Labeler

Deseret Biologicals, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2017-12-15

Marketing end

2023-08-13

Substance

PULSATILLA VULGARIS; EUPHORBIA RESINIFERA RESIN; LUFFA OPERCULATA FRUIT; MERCURIC IODIDE; SILVER NITRATE; CALCIUM SULFIDE; INFLUENZA A VIRUS A/SINGAPORE/GP1908/2015 IVR-180A (H1N1) ANTIGEN (PROPIOLACTONE INACTIVATED); INFLUENZA A VIRUS A/HONG KONG/4801/2014 X-263B (H3N2) ANTIGEN (PROPIOLACTONE INACTIVATED); INFLUENZA B VIRUS B/BRISBANE/60/2008 ANTIGEN (PROPIOLACTONE INACTIVATED); SINUSITISINUM; ASPERGILLUS NIGER VAR. NIGER; CANDIDA ALBICANS; GALLIC ACID MONOHYDRATE; MUCOR RACEMOSUS; ESCHERICHIA COLI

Active strength

2 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record