NDC 66854-003 Gynox-soft
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
PINK (C48328 - PINK)
Product Packages
NDC Code 66854-003-01
Package Description: 210 mL in 1 BOTTLE
NDC Code 66854-003-02
Package Description: 250 mL in 1 BOTTLE
NDC Code 66854-003-03
Package Description: 260 mL in 1 BOTTLE
NDC Code 66854-003-04
Package Description: 270 mL in 1 BOTTLE
NDC Code 66854-003-05
Package Description: 400 mL in 1 BOTTLE
NDC Code 66854-003-06
Package Description: 515 mL in 1 BOTTLE
NDC Code 66854-003-07
Package Description: 1000 mL in 1 BOTTLE
NDC Code 66854-003-09
Package Description: 30 BAG in 1 BOX / 12 mL in 1 BAG (66854-003-08)
NDC Code 66854-003-10
Package Description: 500 mL in 1 BOTTLE
Product Details
What is NDC 66854-003?
What are the uses for Gynox-soft?
Which are Gynox-soft UNII Codes?
The UNII codes for the active ingredients in this product are:
- BORIC ACID (UNII: R57ZHV85D4)
- BORIC ACID (UNII: R57ZHV85D4) (Active Moiety)
Which are Gynox-soft 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)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- COCO GLUCOSIDE (UNII: ICS790225B)
- GLYCERYL OLEATE (UNII: 4PC054V79P)
- CHAMOMILE (UNII: FGL3685T2X)
- PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
* 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".