NDC 57520-0133 Sinus Clear
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57520 - Apotheca Company
- 57520-0133 - Sinus Clear
Product Characteristics
Product Packages
NDC Code 57520-0133-1
Package Description: 30 CAPSULE in 1 BOTTLE
Product Details
What is NDC 57520-0133?
What are the uses for Sinus Clear?
Which are Sinus Clear UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM SULFIDE (UNII: 1MBW07J51Q)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- POTASSIUM DICHROMATE (UNII: T4423S18FM)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- PULSATILLA VULGARIS (UNII: I76KB35JEV)
- PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
Which are Sinus Clear Inactive Ingredients UNII Codes?
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. The UNII codes for the inactive ingredients in this product are:
- ACTAEA CIMICIFUGA ROOT (UNII: 65J267BAZT)
- LICORICE (UNII: 61ZBX54883)
- CNIDIUM ROOT (UNII: 8S3OZD358J)
- ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- MAGNOLIA GRANDIFLORA FLOWER (UNII: RV23PE6426)
- NOTOPTERYGIUM FRANCHETII ROOT (UNII: KRT28P6ITK)
- PLANTAGO SEED (UNII: 9C60Y73166)
- SAPOSHNIKOVIA DIVARICATA ROOT (UNII: 8H84LFK2QD)
- XANTHIUM (UNII: 8555ORT735)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- LIGUSTICUM SINENSE ROOT (UNII: 32SLT970XO)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] 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.
[12] 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".