NDC 81340-001 Cindelight Gel
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Product Details
What is NDC 81340-001?
What are the uses for Cindelight Gel?
Which are Cindelight Gel UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Cindelight Gel 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:
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CITRUS X LIMON LEAF OIL (UNII: E090Y54IT5)
- CALENDULA OFFICINALIS SEED OIL (UNII: 9JS8DS42SV)
- GLYCERIN (UNII: PDC6A3C0OX)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
- PROPYLENE GLYCOL T-BUTYL ETHER (UNII: 03077MV85B)
- CAMELLIA SINENSIS SEED OIL (UNII: O5R6DK2M9K)
- CALLITRIS COLUMELLARIS WOOD OIL (UNII: T9K440NH64)
What is the NDC to RxNorm Crosswalk for Cindelight Gel?
- RxCUI: 581662 - ethanol 70 % Topical Gel
- RxCUI: 581662 - ethanol 0.7 ML/ML Topical Gel
- RxCUI: 581662 - ethyl alcohol 70 % Topical Gel
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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".