ApprovalTrail

Natural health product · NPN 80087522

DROPSORDRY(TM)

Yes: licensed in Canada

The product licence is active. Whether the product is actually on the market is a separate, voluntary notice; the official record shows it.

Licence status Active; licensed August 1, 2018; licence last revised August 22, 2018.
Natural Product Number (NPN)
80087522
Licence holder
CK Ingredients Inc.
Dosage form
Tablet
Route
Oral
Licensing route
Non-Traditional
First licensed
August 1, 2018
Licence last revised
August 22, 2018

Also sold as

Other product names on the same licence.

  • UrgeFreeTM

Medicinal ingredients

Per dosage unit, as licensed.

IngredientAmount
Glycine maxGlycine max - Seed; 22.5 mg aie Isoflavones; 100:1 Dry; equivalent to 5625 mg dried herb56.25 mg
Glycine maxGlycine max - Seed; 9 mg aie Genisteinnot listed
Cucurbita pepoCucurbita pepo - seed; 3.46 % Polyphenols; 10:1 Dry; equivalent to 4457.5 mg dried herb445.75 mg

What it is licensed for

The licence’s own wording. Directions, doses, cautions and warnings are on the official record and the label.

  • DROPSORDRY(TM) helps to decrease nighttime urinary episodes in women due to overactive bladder. DROPSORDRY(TM) helps to reduce urge to urinate and frequency of urination in women due to overactive bladder. DROPSORDRY(TM) helps to relieve symptoms associated with overactive bladder such as nocturia, frequent urination and urgency in women. May reduce severe and frequent menopausal symptoms (such as hot flashes and/or night sweats). DROPSORDRY(TM) helps to reduce frequency of urination at night in men. In general, DROPSORDRY(TM) helps to relief urinary disturbance/symptoms associated with overactive bladder in women.

Non-medicinal ingredients

Magnesium stearate; Silicon dioxide; Titanium dioxide; Microcrystalline cellulose; Stearic acid; Hydroxypropyl Methylcellulose

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