NDC 70486-100 Chi-myst Synergy Topical
NDC Product Code 70486-100
Proprietary Name: Chi-myst Synergy Topical What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
NDC Code Structure
- 70486 - Prescription Care Llc
- 70486-100 - Chi-myst Synergy
NDC 70486-100-00
Package Description: 100 mL in 1 BOTTLE, SPRAY
NDC Product Information
Chi-myst Synergy Topical with NDC 70486-100 is a product labeled by Prescription Care Llc. The generic name of Chi-myst Synergy Topical is . The product's dosage form is and is administered via form.
Labeler Name: Prescription Care Llc
Dosage Form: -
Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
Inactive Ingredient(s)
About the Inactive Ingredient(s)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.
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- LACTIC ACID LACTATE, DL- (UNII: N37QW3EK1L)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
Product Labeler Information
What is the Labeler Name?Name of Company corresponding to the labeler code segment of the Product NDC.
Labeler Name: Prescription Care Llc
Labeler Code: 70486
Start Marketing Date: 06-01-2016 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2018 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.
Exclude Flag: I 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. Values = ‘Y’ or ‘N’.
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