NDC 53346-1334 Dr. Reckeweg R34 Calcossin Combination Product
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What is NDC 53346-1334?
What are the uses for Dr. Reckeweg R34 Calcossin Combination Product?
Which are Dr. Reckeweg R34 Calcossin Combination Product UNII Codes?
The UNII codes for the active ingredients in this product are:
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- CALCIUM FLUORIDE (UNII: O3B55K4YKI)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- CALCIUM HYPOPHOSPHITE (UNII: CUI83R2732)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: O7TSZ97GEP)
- CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J) (Active Moiety)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (Active Moiety)
- HEKLA LAVA (UNII: C21158IIRK)
- HEKLA LAVA (UNII: C21158IIRK) (Active Moiety)
- MERCURIC OXIDE (UNII: IY191986AO)
- MERCURIC OXIDE (UNII: IY191986AO) (Active Moiety)
- DAPHNE MEZEREUM BARK (UNII: X2N6E405GV)
- DAPHNE MEZEREUM BARK (UNII: X2N6E405GV) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
Which are Dr. Reckeweg R34 Calcossin Combination Product 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
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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".