NDC 68703-214 Eczema Remedy
Carbolicum Acidum,Fagopyrum Esculentum,Hydrastis Canadensis,Hydrocotyle Asiatica,Juglans - View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 68703-214?
What are the uses for Eczema Remedy?
What are Eczema Remedy Active Ingredients?
- CENTELLA ASIATICA 30 [hp_X]/113g - A plant of the family APIACEAE which is the source of asiatic acid and asiaticoside. Centella asiatica (L.) Urb. = Hydrocotyle asiatica L. is known for effect on peripheral circulation.
- FAGOPYRUM ESCULENTUM 30 [hp_X]/113g
- HYDRASTIS CANADENSIS WHOLE 30 [hp_X]/113g
- JUGLANS REGIA LEAF 30 [hp_X]/113g
- PHENOL 30 [hp_X]/113g - An antiseptic and disinfectant aromatic alcohol.
- VINCA MINOR 30 [hp_X]/113g - A plant genus of the family Apocynaceae.
Which are Eczema Remedy UNII Codes?
The UNII codes for the active ingredients in this product are:
- FAGOPYRUM ESCULENTUM (UNII: B10M69172N)
- FAGOPYRUM ESCULENTUM (UNII: B10M69172N) (Active Moiety)
- JUGLANS REGIA LEAF (UNII: 85HKB87105)
- JUGLANS REGIA LEAF (UNII: 85HKB87105) (Active Moiety)
- VINCA MINOR (UNII: WGM46PQF02)
- VINCA MINOR (UNII: WGM46PQF02) (Active Moiety)
- HYDRASTIS CANADENSIS WHOLE (UNII: R763EBH88T)
- HYDRASTIS CANADENSIS WHOLE (UNII: R763EBH88T) (Active Moiety)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- CENTELLA ASIATICA (UNII: 7M867G6T1U) (Active Moiety)
- PHENOL (UNII: 339NCG44TV)
- PHENOL (UNII: 339NCG44TV) (Active Moiety)
Which are Eczema Remedy 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:
- WATER (UNII: 059QF0KO0R)
- PHYTOLACCA AMERICANA FRUIT (UNII: WE63661499)
- BLACK OLIVE (UNII: 2M6QWV94OC)
- PEG-8 DIMETHICONE (UNII: GIA7T764OD)
- POLYETHYLENE GLYCOL 700 (UNII: 762678AC5R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- EDETIC ACID (UNII: 9G34HU7RV0)
- COMFREY LEAF (UNII: DG4F8T839X)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- TOCOPHEROL (UNII: R0ZB2556P8)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- AZADIRACHTA INDICA LEAF (UNII: HKY915780T)
- SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SORBIC ACID (UNII: X045WJ989B)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- MACADAMIA ACID (UNII: 7N137Q0QYJ)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
- KUKUI NUT OIL (UNII: TP11QR7B8R)
- LARREA TRIDENTATA LEAF (UNII: PK0TXD049P)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- SALIX ALBA BARK (UNII: 205MXS71H7)
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".