NDC 57955-0305 Syc Miasm

NDC Product Code 57955-0305

NDC 57955-0305-2

Package Description: 59 mL in 1 BOTTLE, SPRAY

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

NDC Product Information

Syc Miasm with NDC 57955-0305 is product labeled by King Bio Inc.. 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.

  • WATER (UNII: 059QF0KO0R)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

Product Labeler Information

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

Labeler Name: King Bio Inc.
Labeler Code: 57955
Start Marketing Date: 01-20-2014 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.

Syc Miasm Product Label Images

Syc Miasm 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

Otc - Active Ingredient

Drug Facts__________________________________________________________________________________________________________HPUS active ingredients: Aconitum napellus, Cantharis, Gelsemium sempervirens, Natrum sulphuricum, Picricum acidum, Pulsatilla, Sepia, Staphysagria. Equal volumes of each ingredient in 10X, 30X, 200X, 1M, LM1, LM2, LM3 potencies.

Indications & Usage

Uses a natural aid for: warts, allergies musculoskeletal aches, rheumatism, candida, yeast, vaginal irritations, herpes, general inflammations of the mucous membranes, sexual excesses.

Inactive Ingredient

Inactive Ingredients:Bio-Energetically Enhanced™ pure water, citric acid and potassium sorbate.

Warnings

  • WarningsStop use and ask a doctor, if symptoms persist or worsen.If pregnant or breast-feeding,  take only on advice of a healthcare professional.

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children

Dosage & Administration

  • Initially, depress pump until primed.​​Spray one dose directly into mouth.Adults 12 and up - 3 sprays 3 times per day.Children 2-12 - 2 sprays 3 times per day.Children 2 mo. - 1 spray 3 times per day

Other Safety Information

Tamper resistant for your protection. Use only if safety seal is intact. This product has not been independently tested.

Otc - Purpose

  • Uses a natural aid for: wartsallergiesmusculoskeletal achesrheumatismcandidayeastvaginal irritationsherpesgeneral inflammations of the mucous membranessexual excesses

* Please review the disclaimer below.