NDC 17089-453

GUNA-COUGH

Althaea Officinalis Leaf - Antimony Potassium Tartrate - Bryonia Alba Root - Cetraria Islandica Subsp. Islandica - Cochineal - Copper - Drosera Rotundifolia - Echinacea Angustifolia - Garden Thyme - Lobaria Pulmonaria - Plantago Major -

GUNA-COUGH is a Oral Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Guna Spa. The primary component is Althaea Officinalis Leaf; Antimony Potassium Tartrate; Bryonia Alba Root; Cetraria Islandica Subsp. Islandica; Cochineal; Copper; Drosera Rotundifolia; Echinacea Angustifolia; Plantago Major; Lobaria Pulmonaria; Thyme.

Product ID17089-453_7df434e5-a06f-2191-e053-2991aa0a5ae7
NDC17089-453
Product TypeHuman Otc Drug
Proprietary NameGUNA-COUGH
Generic NameAlthaea Officinalis Leaf - Antimony Potassium Tartrate - Bryonia Alba Root - Cetraria Islandica Subsp. Islandica - Cochineal - Copper - Drosera Rotundifolia - Echinacea Angustifolia - Garden Thyme - Lobaria Pulmonaria - Plantago Major -
Dosage FormSolution/ Drops
Route of AdministrationORAL
Marketing Start Date2010-05-27
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameGuna spa
Substance NameALTHAEA OFFICINALIS LEAF; ANTIMONY POTASSIUM TARTRATE; BRYONIA ALBA ROOT; CETRARIA ISLANDICA SUBSP. ISLANDICA; COCHINEAL; COPPER; DROSERA ROTUNDIFOLIA; ECHINACEA ANGUSTIFOLIA; PLANTAGO MAJOR; LOBARIA PULMONARIA; THYME
Active Ingredient Strength1 [hp_X]/150mL; [hp_X]/150mL; [hp_X]/150mL; [hp_X]/150mL; [hp_X]/150mL; [hp_X]/150mL; [hp_X]/150mL; [hp_X]/150mL; [hp_X]/150mL; [hp_X]/150mL; [hp_X]/150mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 17089-453-24

1 BOTTLE in 1 BOX (17089-453-24) > 150 mL in 1 BOTTLE
Marketing Start Date2018-04-09
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 17089-453-24 [17089045324]

GUNA-COUGH SOLUTION/ DROPS
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-04-09
Inactivation Date2020-01-31
Reactivation Date2020-03-13

Drug Details

Active Ingredients

IngredientStrength
ALTHAEA OFFICINALIS LEAF1 [hp_X]/150mL

OpenFDA Data

SPL SET ID:40e9509c-5cc2-4077-ab89-34bec9015f42
Manufacturer
UNII
UPC Code
  • 0317089453246
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