NDC 82341-302 Onsaemiro Damda
Anotec 0307,Cypress Water,Houttuynia Cordata Eextract,Glycerin Liquid Topical - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 82341-302?
What are the uses for Onsaemiro Damda?
What are Onsaemiro Damda Active Ingredients?
- ALCOHOL 30 mL/100mL
- CHAMAECYPARIS OBTUSA WHOLE 25 g/100mL
- EUCALYPTUS OIL .3 g/100mL - An oily liquid that is extracted from the leaves of EUCALYPTUS trees.
- GLYCERIN .1 g/100mL
- HOUTTUYNIA CORDATA FLOWERING TOP 5 g/100mL
- OLIVE OIL .3 g/100mL - Oil extracted from fruit of the OLIVE TREE (genus Olea).
- SORBITOL .3 g/100mL - A polyhydric alcohol with about half the sweetness of sucrose. Sorbitol occurs naturally and is also produced synthetically from glucose. It was formerly used as a diuretic and may still be used as a laxative and in irrigating solutions for some surgical procedures. It is also used in many manufacturing processes, as a pharmaceutical aid, and in several research applications.
- WHITE PINE OIL .3 g/100mL
Which are Onsaemiro Damda UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
- HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22) (Active Moiety)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
- CHAMAECYPARIS OBTUSA WHOLE (UNII: 80ZNL1G5XY)
- CHAMAECYPARIS OBTUSA WHOLE (UNII: 80ZNL1G5XY) (Active Moiety)
- WHITE PINE OIL (UNII: HA5CX6676U)
- WHITE PINE OIL (UNII: HA5CX6676U) (Active Moiety)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- OLIVE OIL (UNII: 6UYK2W1W1E) (Active Moiety)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- EUCALYPTUS OIL (UNII: 2R04ONI662) (Active Moiety)
- SORBITOL (UNII: 506T60A25R)
- SORBITOL (UNII: 506T60A25R) (Active Moiety)
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Onsaemiro Damda 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)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- TEA TREE OIL (UNII: VIF565UC2G)
- LEMON OIL (UNII: I9GRO824LL)
Which are the Pharmacologic Classes for Onsaemiro Damda?
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Glycerol - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Lipid Emulsion - [EPC] (Established Pharmacologic Class)
- Lipids - [CS]
- Non-Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
* 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".