NDC 77818-305 Cellamo Phytoboosting Tonic
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What is NDC 77818-305?
What are the uses for Cellamo Phytoboosting Tonic?
Which are Cellamo Phytoboosting Tonic UNII Codes?
The UNII codes for the active ingredients in this product are:
- ELEUTHEROCOCCUS NODIFLORUS ROOT BARK (UNII: W7PRK433YB)
- ELEUTHEROCOCCUS NODIFLORUS ROOT BARK (UNII: W7PRK433YB) (Active Moiety)
- HORDEUM VULGARE WHOLE (UNII: 8JBE478M5Q)
- HORDEUM VULGARE WHOLE (UNII: 8JBE478M5Q) (Active Moiety)
- LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
- LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y) (Active Moiety)
- VITEX TRIFOLIA FRUIT (UNII: Q04E1F5351)
- VITEX TRIFOLIA FRUIT (UNII: Q04E1F5351) (Active Moiety)
- ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF)
- ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF) (Active Moiety)
- RAPHANUS SATIVUS VAR. SATIVUS SEED (UNII: A94I086Q5E)
- RAPHANUS SATIVUS VAR. SATIVUS SEED (UNII: A94I086Q5E) (Active Moiety)
- CHINESE CINNAMON (UNII: WS4CQ062KM)
- CHINESE CINNAMON (UNII: WS4CQ062KM) (Active Moiety)
- ARCTIUM LAPPA FRUIT (UNII: EA541308MV)
- ARCTIUM LAPPA FRUIT (UNII: EA541308MV) (Active Moiety)
Which are Cellamo Phytoboosting Tonic 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:
- PULSATILLA KOREANA ROOT (UNII: FY35I16MPL)
- USNEA BARBATA (UNII: D6DVA9TCAP)
- ZANTHOXYLUM PIPERITUM FRUIT PULP (UNII: 7PFC2VA251)
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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".