NDC 57955-0815 Mole Remover
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57955 - King Bio Inc.
- 57955-0815 - Mole Remover
Product Packages
NDC Code 57955-0815-3
Package Description: 1 BOTTLE, WITH APPLICATOR in 1 CARTON / 15 mL in 1 BOTTLE, WITH APPLICATOR
Product Details
What is NDC 57955-0815?
What are the uses for Mole Remover?
Which are Mole Remover UNII Codes?
The UNII codes for the active ingredients in this product are:
- CARBO ANIMALIS (UNII: 279O8I0433)
- CARBO ANIMALIS (UNII: 279O8I0433) (Active Moiety)
- GRAPHITE (UNII: 4QQN74LH4O)
- GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
Which are Mole Remover 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:
- ALCOHOL (UNII: 3K9958V90M)
- CASTOR OIL (UNII: D5340Y2I9G)
- CEDAR LEAF OIL (UNII: BJ169U4NLG)
- FRANKINCENSE OIL (UNII: 67ZYA5T02K)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- OREGANO LEAF OIL (UNII: 7D0CGR40U1)
- TEA TREE OIL (UNII: VIF565UC2G)
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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".