NDC 69353-001 Singiso

NDC Product Code 69353-001

NDC CODE: 69353-001

Proprietary Name: Singiso What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

NDC Code Structure

  • 69353 - Fda Trading Co.,ltd.

NDC 69353-001-01

Package Description: 30 TABLET in 1 BOX

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Singiso with NDC 69353-001 is a product labeled by Fda Trading Co.,ltd.. The product's dosage form is and is administered via form.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • TURNERA DIFFUSA LEAF (UNII: 812R0W1I3K)
  • SOY PROTEIN (UNII: R44IWB3RN5)
  • CORDYCEPS GUNNII FRUITING BODY (UNII: D11BQN236E)
  • CORNUS OFFICINALIS FRUIT (UNII: 23NL8NQ187)
  • LYCIUM BARBARUM FRUIT (UNII: 930626MWDL)
  • ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF)
  • CYNANCHUM STAUNTONII ROOT (UNII: 2A4Y8J8BVJ)
  • LEPIDIUM MEYENII WHOLE (UNII: 94866V8426)
  • LACTOSE (UNII: J2B2A4N98G)
  • ARGININE (UNII: 94ZLA3W45F)
  • LYSINE HYDROCHLORIDE (UNII: JNJ23Q2COM)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • HYPROMELLOSES (UNII: 3NXW29V3WO)
  • SUCROSE (UNII: C151H8M554)
  • ZINC OXIDE (UNII: SOI2LOH54Z)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Fda Trading Co.,ltd.
Labeler Code: 69353
Start Marketing Date: 11-15-2014 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2018 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Singiso Product Label Images

Singiso Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

Red ginseng 15.63%

Otc - Purpose

Stimulant

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Uses

To help the treatment and prevention of blood circulation, prostate, erectile dysfunction.

Warning

If you take any serious medications or medical condition, consult your doctor

Direction

Take 1 tablet a day (after having dinner, before sleep)

Other Information

  • Keep product out of direct sunlight, high temperature and humidity. Store in a cool dry place. Any times past the expiration date or damaged in transit can be exchanged where you originally purchased the item.

Other

CAUTION:Do not exceed the recommended dosage.To assure freshness and potency, store at room temperature 15°C - 30°CStore away from heat, light and moisture, if you are pregnant, nursing, taking any medication or have a medical condition, please consult your healthcare practitioner before taking any dietary supplement.

* Please review the disclaimer below.