NDC 17089-472

GUNA SINUS PLUS

Althaea Officinalis Leaf - Calcium Sulfide - Copper - Drimia Maritima Bulb - Echinacea Angustifolia - Hydrastis Canadensis Whole - Lobaria Pulmonaria - Manganese - Mercuric Sulfide - Onion - Plantago Major Whole - Potassium Dichromate - Pulsatilla Vulgaris - Silicon Dioxide - Silver Nitrate - Sinusitisinum - Sus Scrofa Nasal Mucosa -

GUNA SINUS PLUS is a Nasal Spray in the Human Otc Drug category. It is labeled and distributed by Guna Spa. The primary component is Onion; Althaea Officinalis Leaf; Silver Nitrate; Ascorbic Acid; Hydrastis Canadensis Whole; Lobaria Pulmonaria; Copper; Echinacea Angustifolia; Calcium Sulfide; Potassium Dichromate; Manganese; Mercuric Sulfide; Sus Scrofa Nasal Mucosa; Pulsatilla Vulgaris; Silicon Dioxide; Sinusitisinum; Plantago Major Whole; Drimia Maritima Bulb.

Product ID17089-472_b48c5634-24d0-343e-e053-2995a90a3a9a
NDC17089-472
Product TypeHuman Otc Drug
Proprietary NameGUNA SINUS PLUS
Generic NameAlthaea Officinalis Leaf - Calcium Sulfide - Copper - Drimia Maritima Bulb - Echinacea Angustifolia - Hydrastis Canadensis Whole - Lobaria Pulmonaria - Manganese - Mercuric Sulfide - Onion - Plantago Major Whole - Potassium Dichromate - Pulsatilla Vulgaris - Silicon Dioxide - Silver Nitrate - Sinusitisinum - Sus Scrofa Nasal Mucosa -
Dosage FormSpray
Route of AdministrationNASAL
Marketing Start Date2021-02-17
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameGuna spa
Substance NameONION; ALTHAEA OFFICINALIS LEAF; SILVER NITRATE; ASCORBIC ACID; HYDRASTIS CANADENSIS WHOLE; LOBARIA PULMONARIA; COPPER; ECHINACEA ANGUSTIFOLIA; CALCIUM SULFIDE; POTASSIUM DICHROMATE; MANGANESE; MERCURIC SULFIDE; SUS SCROFA NASAL MUCOSA; PULSATILLA VULGARIS; SILICON DIOXIDE; SINUSITISINUM; PLANTAGO MAJOR WHOLE; DRIMIA MARITIMA BULB
Active Ingredient Strength6 [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 17089-472-23

1 BOTTLE, SPRAY in 1 BOX (17089-472-23) > 30 mL in 1 BOTTLE, SPRAY
Marketing Start Date2021-02-17
NDC Exclude FlagN
Sample Package?N

Drug Details


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