NDC 61995-1302 Av3630200 Avalon Organics Eczema Relief Gentle Cleanser
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61995 - The Hain Celestial Group, Inc.
- 61995-1302 - Av3630200 Avalon Organics Eczema Relief Gentle Cleanser
Product Packages
NDC Code 61995-1302-8
Package Description: 325 g in 1 BOTTLE, PLASTIC
Product Details
What is NDC 61995-1302?
What are the uses for Av3630200 Avalon Organics Eczema Relief Gentle Cleanser?
Which are Av3630200 Avalon Organics Eczema Relief Gentle Cleanser UNII Codes?
The UNII codes for the active ingredients in this product are:
- OATMEAL (UNII: 8PI54V663Y)
- OATMEAL (UNII: 8PI54V663Y) (Active Moiety)
Which are Av3630200 Avalon Organics Eczema Relief Gentle Cleanser 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:
- CALCIUM GLUCONATE (UNII: SQE6VB453K)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- COCONUT OIL (UNII: Q9L0O73W7L)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- DISODIUM COCOYL GLUTAMATE (UNII: MBK0CP8F5A)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- LINSEED OIL (UNII: 84XB4DV00W)
- GLYCERYL LAURATE (UNII: Y98611C087)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
What is the NDC to RxNorm Crosswalk for Av3630200 Avalon Organics Eczema Relief Gentle Cleanser?
- RxCUI: 1486782 - colloidal oatmeal 1.5 % Topical Lotion
- RxCUI: 1486782 - colloidal oatmeal 15 MG/ML Topical Lotion
* 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".