NDC 69697-982 Q2 Oral Care Kit With Chg
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69697 - Halyard Health
- 69697-982 - Q2 Oral Care Kit With Chg
Product Characteristics
PEPPERMINT (C73408)
Product Packages
NDC Code 69697-982-01
Package Description: 1 KIT in 1 CARTON * 14 mL in 1 CUP, UNIT-DOSE * 10 g in 1 TUBE * 10 CUP, UNIT-DOSE in 1 TRAY (50383-720-15) / 15 mL in 1 CUP, UNIT-DOSE * 14 mL in 1 CUP, UNIT-DOSE (69697-991-01)
Product Details
What is NDC 69697-982?
What are the uses for Q2 Oral Care Kit With Chg?
Which are Q2 Oral Care Kit With Chg UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V) (Active Moiety)
- CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
- CHLORHEXIDINE (UNII: R4KO0DY52L) (Active Moiety)
Which are Q2 Oral Care Kit With Chg 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- MINT (UNII: FV98Z8GITP)
- SACCHARIN SODIUM DIHYDRATE (UNII: SB8ZUX40TY)
- ALCOHOL (UNII: 3K9958V90M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- PEG-40 SORBITAN DIISOSTEARATE (UNII: JL4CCU7I1G)
What is the NDC to RxNorm Crosswalk for Q2 Oral Care Kit With Chg?
- RxCUI: 834127 - chlorhexidine gluconate 0.12 % Oral Rinse
- RxCUI: 834127 - chlorhexidine gluconate 1.2 MG/ML Mouthwash
- RxCUI: 834127 - chlorhexidine gluconate 0.12 % Mouthwash
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[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".