NDC 72275-733 Acyclovix
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72275 - Primary Pharmaceuticals, Inc.
- 72275-733 - Acyclovix
Product Characteristics
Product Packages
NDC Code 72275-733-77
Package Description: 1 KIT in 1 CARTON * 7.1 g in 1 TUBE * 100 CAPSULE in 1 BOTTLE
Product Details
What is NDC 72275-733?
What are the uses for Acyclovix?
Which are Acyclovix UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BENZYL ALCOHOL (UNII: LKG8494WBH) (Active Moiety)
- ACYCLOVIR (UNII: X4HES1O11F)
- ACYCLOVIR (UNII: X4HES1O11F) (Active Moiety)
Which are Acyclovix 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:
- BORIC ACID (UNII: R57ZHV85D4)
- EUCALYPTOL (UNII: RV6J6604TK)
- THYMOL (UNII: 3J50XA376E)
- MENTHOL (UNII: L7T10EIP3A)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- ALCOHOL (UNII: 3K9958V90M)
- TANNIC ACID (UNII: 28F9E0DJY6)
- WATER (UNII: 059QF0KO0R)
- HYDROXYPROPYL CELLULOSE (TYPE M) (UNII: U3JF91U133)
- STARCH, CORN (UNII: O8232NY3SJ)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
What is the NDC to RxNorm Crosswalk for Acyclovix?
- RxCUI: 197310 - acyclovir 200 MG Oral Capsule
- RxCUI: 197310 - acycycloguanosine 200 MG Oral Capsule
- RxCUI: 581456 - benzyl alcohol 10 % Oral Gel
- RxCUI: 581456 - benzyl alcohol 0.1 ML/ML Oral Gel
- RxCUI: 581456 - benzyl alcohol 10 % Mucous Membrane Topical Gel
* 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".