NDC 76479-4403 Eco.kid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76479 - Fravin Pty Ltd
- 76479-4403 - Eco.kid
Product Packages
NDC Code 76479-4403-1
Package Description: 1 BOTTLE in 1 CARTON / 59 mL in 1 BOTTLE
Product Details
What is NDC 76479-4403?
What are the uses for Eco.kid?
Which are Eco.kid UNII Codes?
The UNII codes for the active ingredients in this product are:
- PIPERONYL BUTOXIDE (UNII: LWK91TU9AH)
- PIPERONYL BUTOXIDE (UNII: LWK91TU9AH) (Active Moiety)
- PYRETHRUM EXTRACT (UNII: ZUM06L90GV)
- PYRETHRUM EXTRACT (UNII: ZUM06L90GV) (Active Moiety)
Which are Eco.kid 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:
- COCONUT OIL (UNII: Q9L0O73W7L)
- ORANGE OIL (UNII: AKN3KSD11B)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- GLYCERIN (UNII: PDC6A3C0OX)
- SOYBEAN OIL (UNII: 241ATL177A)
- LEPTOSPERMUM PETERSONII LEAF OIL (UNII: N37UWG52T3)
- MAURITIA FLEXUOSA FRUIT OIL (UNII: 48H19MS04L)
- TEA TREE OIL (UNII: VIF565UC2G)
- MELALEUCA QUINQUENERVIA LEAF OIL (UNII: 22K2F1YSHD)
What is the NDC to RxNorm Crosswalk for Eco.kid?
- RxCUI: 1232410 - piperonyl butoxide 2 % / pyrethrum extract 0.17 % Medicated Shampoo
- RxCUI: 1232410 - piperonyl butoxide 20 MG/ML / pyrethrum extract 1.7 MG/ML Medicated Shampoo
* 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".