NDC 79061-042 Pro Clear Foam
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 79061-042?
What are the uses for Pro Clear Foam?
Which are Pro Clear Foam UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Pro Clear Foam 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)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- PHELLODENDRON AMURENSE BARK (UNII: PBG27B754G)
- PEAR JUICE (UNII: F214DLA9BE)
- REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ)
- HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
- AZADIRACHTA INDICA LEAF (UNII: HKY915780T)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- SOYBEAN (UNII: L7HT8F1ZOD)
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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".