NDC 64058-145 Miracle Plus Diabetic Homeopathic Nerve Pain Reliever
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64058 - Concept Laboratories, Inc.
- 64058-145 - Miracle Plus Diabetic Homeopathic
Product Packages
NDC Code 64058-145-21
Package Description: 5 mL in 1 BOTTLE
Product Details
What is NDC 64058-145?
What are the uses for Miracle Plus Diabetic Homeopathic Nerve Pain Reliever?
Which are Miracle Plus Diabetic Homeopathic Nerve Pain Reliever UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACONITUM NAPELLUS (UNII: U0NQ8555JD)
- ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N)
- CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N) (Active Moiety)
Which are Miracle Plus Diabetic Homeopathic Nerve Pain Reliever 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)
- APRICOT KERNEL OIL (UNII: 54JB35T06A)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- TEA TREE OIL (UNII: VIF565UC2G)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- GERANIUM OIL, ALGERIAN TYPE (UNII: 5Q1I94P4WG)
- BERGAMOT OIL (UNII: 39W1PKE3JI)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
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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".