NDC 57240-2027 Zippity Doos Styling For Children
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 57240-2027?
What are the uses for Zippity Doos Styling For Children?
Which are Zippity Doos Styling For Children UNII Codes?
The UNII codes for the active ingredients in this product are:
- ROSEMARY (UNII: IJ67X351P9)
- ROSEMARY (UNII: IJ67X351P9) (Active Moiety)
Which are Zippity Doos Styling For Children 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)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PRUNUS SEROTINA BARK (UNII: 5D48E975HA)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- LAVANDULA ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)
- CYMBOPOGON SCHOENANTHUS TOP (UNII: 9SJI1LW39W)
- GERANIUM MACULATUM ROOT (UNII: 93IXI5B6OJ)
- MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- ASPARTIC ACID (UNII: 30KYC7MIAI)
- GLUTAMIC ACID (UNII: 3KX376GY7L)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- TEA TREE OIL (UNII: VIF565UC2G)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- CITRONELLA OIL (UNII: QYO8Q067D0)
- SPEARMINT OIL (UNII: C3M81465G5)
- EDETATE SODIUM (UNII: MP1J8420LU)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
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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".