NDC 44911-0528 Chemstat
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 44911 - Energique, Inc.
- 44911-0528 - Chemstat
Product Packages
NDC Code 44911-0528-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 44911-0528?
What are the uses for Chemstat?
Which are Chemstat UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
- TARAXACUM OFFICINALE (UNII: 39981FM375)
- TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (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)
- KEROSENE (UNII: 1C89KKC04E)
- KEROSENE (UNII: 1C89KKC04E) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- ASPIRIN (UNII: R16CO5Y76E)
- ASPIRIN (UNII: R16CO5Y76E) (Active Moiety)
- NITROGLYCERIN (UNII: G59M7S0WS3)
- NITROGLYCERIN (UNII: G59M7S0WS3) (Active Moiety)
- INSULIN PORK (UNII: AVT680JB39)
- INSULIN PORK (UNII: AVT680JB39) (Active Moiety)
- LITHIUM CARBONATE (UNII: 2BMD2GNA4V)
- LITHIUM CATION (UNII: 8H8Z5UER66) (Active Moiety)
- THYROID, PORCINE (UNII: 6RV024OAUQ)
- THYROID, PORCINE (UNII: 6RV024OAUQ) (Active Moiety)
- ACETIC ACID (UNII: Q40Q9N063P)
- ACETIC ACID (UNII: Q40Q9N063P) (Active Moiety)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- BENZOIC ACID (UNII: 8SKN0B0MIM) (Active Moiety)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BENZYL ALCOHOL (UNII: LKG8494WBH) (Active Moiety)
- BORIC ACID (UNII: R57ZHV85D4)
- BORIC ACID (UNII: R57ZHV85D4) (Active Moiety)
- CHLORINE (UNII: 4R7X1O2820)
- CHLORINE (UNII: 4R7X1O2820) (Active Moiety)
- CORTISONE ACETATE (UNII: 883WKN7W8X)
- CORTISONE (UNII: V27W9254FZ) (Active Moiety)
- EUGENOL (UNII: 3T8H1794QW)
- EUGENOL (UNII: 3T8H1794QW) (Active Moiety)
- ESTRONE (UNII: 2DI9HA706A)
- ESTRONE (UNII: 2DI9HA706A) (Active Moiety)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) (Active Moiety)
- LACTIC ACID, DL- (UNII: 3B8D35Y7S4)
- LACTIC ACID, DL- (UNII: 3B8D35Y7S4) (Active Moiety)
- PETROLATUM (UNII: 4T6H12BN9U)
- PETROLATUM (UNII: 4T6H12BN9U) (Active Moiety)
- PHENYLBUTAZONE (UNII: GN5P7K3T8S)
- PHENYLBUTAZONE (UNII: GN5P7K3T8S) (Active Moiety)
- LEAD (UNII: 2P299V784P)
- LEAD (UNII: 2P299V784P) (Active Moiety)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SORBIC ACID (UNII: X045WJ989B) (Active Moiety)
- RESORCINOL (UNII: YUL4LO94HK)
- RESORCINOL (UNII: YUL4LO94HK) (Active Moiety)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- SORBITOL (UNII: 506T60A25R)
- SORBITOL (UNII: 506T60A25R) (Active Moiety)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y) (Active Moiety)
- XYLITOL (UNII: VCQ006KQ1E)
- XYLITOL (UNII: VCQ006KQ1E) (Active Moiety)
- CORTICOTROPIN (UNII: K0U68Q2TXA)
- CORTICOTROPIN (UNII: K0U68Q2TXA) (Active Moiety)
Which are Chemstat 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".