NDC 50845-0249 Metals
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50845 - Liddell Laboratories, Inc.
- 50845-0249 - Metals
Product Packages
NDC Code 50845-0249-2
Package Description: 1 BOTTLE, SPRAY in 1 CARTON / 30 mL in 1 BOTTLE, SPRAY (50845-0249-1)
Product Details
What is NDC 50845-0249?
What are the uses for Metals?
Which are Metals UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ALUMINUM OXIDE (UNII: LMI26O6933) (Active Moiety)
- GOLD (UNII: 79Y1949PYO)
- GOLD (UNII: 79Y1949PYO) (Active Moiety)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (Active Moiety)
- CAUSTICUM (UNII: DD5FO1WKFU)
- CAUSTICUM (UNII: DD5FO1WKFU) (Active Moiety)
- CYSTEINE (UNII: K848JZ4886)
- CYSTEINE (UNII: K848JZ4886) (Active Moiety)
- PORK LIVER (UNII: 6EC706HI7F)
- PORK LIVER (UNII: 6EC706HI7F) (Active Moiety)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
- NITRIC ACID (UNII: 411VRN1TV4)
- NITRIC ACID (UNII: 411VRN1TV4) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- PLATINUM (UNII: 49DFR088MY)
- PLATINUM (UNII: 49DFR088MY) (Active Moiety)
- TIN (UNII: 387GMG9FH5)
- TIN (UNII: 387GMG9FH5) (Active Moiety)
- STILLINGIA SYLVATICA ROOT (UNII: QBR70R4FBK)
- STILLINGIA SYLVATICA ROOT (UNII: QBR70R4FBK) (Active Moiety)
- TELLURIUM (UNII: NQA0O090ZJ)
- TELLURIUM (UNII: NQA0O090ZJ) (Active Moiety)
- ALCOHOL, X-RAY EXPOSED (1000 RAD) (UNII: 6PRJ93602P)
- ALCOHOL, X-RAY EXPOSED (1000 RAD) (UNII: 6PRJ93602P) (Active Moiety)
Which are Metals 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
* Please review the disclaimer below.
[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".