NDC 61995-1301 Av3630100 Avalon Organics Eczema Relief Body
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What is NDC 61995-1301?
What are the uses for Av3630100 Avalon Organics Eczema Relief Body?
Which are Av3630100 Avalon Organics Eczema Relief Body UNII Codes?
The UNII codes for the active ingredients in this product are:
- OATMEAL (UNII: 8PI54V663Y)
- OATMEAL (UNII: 8PI54V663Y) (Active Moiety)
Which are Av3630100 Avalon Organics Eczema Relief Body 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:
- SAFFLOWER OIL (UNII: 65UEH262IS)
- SHEA BUTTER (UNII: K49155WL9Y)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- ARGININE (UNII: 94ZLA3W45F)
- 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)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- LINSEED OIL (UNII: 84XB4DV00W)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- DOCOSANOL (UNII: 9G1OE216XY)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
What is the NDC to RxNorm Crosswalk for Av3630100 Avalon Organics Eczema Relief Body?
- RxCUI: 1654721 - colloidal oatmeal 1.5 % Topical Cream
- RxCUI: 1654721 - colloidal oatmeal 15 MG/ML Topical Cream
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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".