NDC 63083-5018 Pneumo Drops 5018
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-5018 - Pneumo Drops
Product Packages
NDC Code 63083-5018-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-5018?
What are the uses for Pneumo Drops 5018?
Which are Pneumo Drops 5018 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TEUCRIUM SCORODONIA FLOWERING TOP (UNII: LOK3I16O7G)
- TEUCRIUM SCORODONIA FLOWERING TOP (UNII: LOK3I16O7G) (Active Moiety)
- EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z)
- EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z) (Active Moiety)
- OENANTHE AQUATICA FRUIT (UNII: N4LEE4Z93J)
- OENANTHE AQUATICA FRUIT (UNII: N4LEE4Z93J) (Active Moiety)
- ARSENIC TRIIODIDE (UNII: 3029988O2T)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- BEEF LUNG (UNII: 2I1RTO1MBR)
- BEEF LUNG (UNII: 2I1RTO1MBR) (Active Moiety)
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J) (Active Moiety)
- TIN (UNII: 387GMG9FH5)
- TIN (UNII: 387GMG9FH5) (Active Moiety)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Pneumo Drops 5018 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)
* 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".