NDC 35781-0210 Speedgel Rx
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 35781 - Gensco Laboratories, Llc
- 35781-0210 - Speedgel Rx
Product Packages
NDC Code 35781-0210-1
Package Description: 1 BOTTLE, DISPENSING in 1 CARTON / 10 mL in 1 BOTTLE, DISPENSING
NDC Code 35781-0210-2
Package Description: 1 BOTTLE, DISPENSING in 1 CARTON / 30 mL in 1 BOTTLE, DISPENSING
NDC Code 35781-0210-9
Package Description: 1 BOTTLE, DISPENSING in 1 CARTON / 90 mL in 1 BOTTLE, DISPENSING
Product Details
What is NDC 35781-0210?
What are the uses for Speedgel Rx?
Which are Speedgel Rx UNII Codes?
The UNII codes for the active ingredients in this product are:
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- ECHINACEA PURPUREA (UNII: QI7G114Y98) (Active Moiety)
- ACONITUM NAPELLUS (UNII: U0NQ8555JD)
- ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
- BELLIS PERENNIS (UNII: 2HU33I03UY)
- BELLIS PERENNIS (UNII: 2HU33I03UY) (Active Moiety)
- CHAMOMILE (UNII: FGL3685T2X)
- CHAMOMILE (UNII: FGL3685T2X) (Active Moiety)
- ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)
- ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) (Active Moiety)
- HYPERICUM OIL (UNII: OZU2FC70HY)
- HYPERICUM OIL (UNII: OZU2FC70HY) (Active Moiety)
- COMFREY ROOT (UNII: M9VVZ08EKQ)
- COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
- COLCHICINE (UNII: SML2Y3J35T)
- COLCHICINE (UNII: SML2Y3J35T) (Active Moiety)
- GINGER (UNII: C5529G5JPQ)
- GINGER (UNII: C5529G5JPQ) (Active Moiety)
Which are Speedgel Rx 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)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- UREA (UNII: 8W8T17847W)
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
* 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".