NDC 57240-2010 Zippity Doos Conditioner For Children
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 57240-2010?
What are the uses for Zippity Doos Conditioner For Children?
Which are Zippity Doos Conditioner For Children UNII Codes?
The UNII codes for the active ingredients in this product are:
- ROSEMARY OIL (UNII: 8LGU7VM393)
- ROSEMARY OIL (UNII: 8LGU7VM393) (Active Moiety)
Which are Zippity Doos Conditioner 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)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- GLYCERIN (UNII: PDC6A3C0OX)
- GERANIUM MACULATUM ROOT (UNII: 93IXI5B6OJ)
- CITRONELLA OIL (UNII: QYO8Q067D0)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- TEA TREE OIL (UNII: VIF565UC2G)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- PRUNUS SEROTINA BARK (UNII: 5D48E975HA)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CETRIMONIUM BROMIDE (UNII: L64N7M9BWR)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- TROLAMINE (UNII: 9O3K93S3TK)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- D&C VIOLET NO. 2 (UNII: 350KA7O6HK)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
* 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".