NDC 69804-064 Extra Strength Scar Prevention
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69804 - Ridge Properties
- 69804-064 - Extra Strength Scar Prevention
Product Packages
NDC Code 69804-064-01
Package Description: 56700 mg in 1 BOTTLE, SPRAY
NDC Code 69804-064-04
Package Description: 113400 mg in 1 BOTTLE, SPRAY
NDC Code 69804-064-07
Package Description: 28500 mg in 1 BOTTLE, SPRAY
NDC Code 69804-064-08
Package Description: 14200 mg in 1 BOTTLE, SPRAY
Product Details
What is NDC 69804-064?
Which are Extra Strength Scar Prevention UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Extra Strength Scar Prevention 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:
- WITCH HAZEL (UNII: 101I4J0U34)
- PIPER METHYSTICUM WHOLE (UNII: 3P306S300W)
- ACHILLEA MILLEFOLIUM OIL (UNII: 97P5D0WG43)
- COPAIBA OIL (UNII: 64VX45Y68N)
- NUTMEG OIL (UNII: Z1CLM48948)
What is the NDC to RxNorm Crosswalk for Extra Strength Scar Prevention?
- RxCUI: 1045432 - lidocaine HCl 4 % Topical Spray
- RxCUI: 1045432 - lidocaine hydrochloride 40 MG/ML Topical Spray
- RxCUI: 1045432 - lidocaine HCl 4 % Topical Spray Gel
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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".