NDC 14783-437 Lbel Dry Effect 48
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 14783 - Ventura International Ltd
- 14783-437 - Lbel
Product Packages
NDC Code 14783-437-01
Package Description: 125 mL in 1 CAN
Product Details
What is NDC 14783-437?
What are the uses for Lbel Dry Effect 48?
Which are Lbel Dry Effect 48 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M)
- ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (Active Moiety)
Which are Lbel Dry Effect 48 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:
- BUTANE (UNII: 6LV4FOR43R)
- ISOBUTANE (UNII: BXR49TP611)
- PROPANE (UNII: T75W9911L6)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- WATER (UNII: 059QF0KO0R)
- TRICLOSAN (UNII: 4NM5039Y5X)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- BOMBYX MORI FIBER (UNII: 6LK42KUV6W)
- EUROPEAN HAZELNUT OIL (UNII: 8RQ2839AVG)
- WHEAT GERM OIL (UNII: 14C97E680P)
- LEMON PEEL (UNII: 72O054U628)
- CINNAMON BARK OIL (UNII: XE54U569EC)
- LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- MENTHA PIPERITA LEAF (UNII: A389O33LX6)
- OLEA EUROPAEA LEAF (UNII: MJ95C3OH47)
- OREGANO (UNII: 0E5AT8T16U)
- ROSEMARY (UNII: IJ67X351P9)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- STARCH, CORN (UNII: O8232NY3SJ)
- MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
- THYME (UNII: CW657OBU4N)
- ALMOND OIL (UNII: 66YXD4DKO9)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- HYPERICUM PERFORATUM FLOWER (UNII: A6V4CUE7PV)
- BORAGO OFFICINALIS SEED (UNII: 2GXJ790US0)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
* 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".