NDC 61995-4704 Earth Best Diaper Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61995 - The Hain Celestial Group, Inc
- 61995-4704 - Earth Best Diaper Relief
Product Packages
NDC Code 61995-4704-4
Package Description: 113 g in 1 TUBE
Product Details
What is NDC 61995-4704?
What are the uses for Earth Best Diaper Relief?
Which are Earth Best Diaper Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Earth Best Diaper Relief 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CHAMOMILE (UNII: FGL3685T2X)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- GLYCERYL MONOBEHENATE (UNII: A626UU0W2A)
- GLYCERYL DIBEHENATE (UNII: R8WTH25YS2)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- JOJOBA OIL (UNII: 724GKU717M)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- YELLOW WAX (UNII: 2ZA36H0S2V)
What is the NDC to RxNorm Crosswalk for Earth Best Diaper Relief?
- RxCUI: 1727722 - zinc oxide 19 % Topical Ointment
- RxCUI: 1727722 - zinc oxide 19 MG/MG Topical Ointment
- RxCUI: 1727722 - zinc oxide 190 MG per GM Topical Ointment
- RxCUI: 1727722 - ZNO 19 MG/MG Topical Ointment
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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".