NDC 60512-6009 Eczema Real Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 60512 - Homeolab Usa Inc.
- 60512-6009 - Eczema
Product Characteristics
Product Packages
NDC Code 60512-6009-0
Package Description: 90 TABLET, CHEWABLE in 1 BOTTLE
Product Details
What is NDC 60512-6009?
What are the uses for Eczema Real Relief?
Which are Eczema Real Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- FUMARIA OFFICINALIS FLOWERING TOP (UNII: VH659J61ZL)
- FUMARIA OFFICINALIS FLOWERING TOP (UNII: VH659J61ZL) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY (UNII: DIF093I037)
- AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY (UNII: DIF093I037) (Active Moiety)
- KEROSENE (UNII: 1C89KKC04E)
- KEROSENE (UNII: 1C89KKC04E) (Active Moiety)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (Active Moiety)
- POTASSIUM ARSENITE ANHYDROUS (UNII: BM2U42PAKI)
- ARSENITE ION (UNII: N5509X556J) (Active Moiety)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ALUMINUM OXIDE (UNII: LMI26O6933) (Active Moiety)
Which are Eczema Real 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:
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
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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".