NDC 54111-152 Naturopathica
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54111 - Bentley Laboratories, Llc
- 54111-152 - Naturopathica
Product Packages
NDC Code 54111-152-50
Package Description: 1 JAR in 1 CARTON / 50 mL in 1 JAR
NDC Code 54111-152-51
Package Description: 1 JAR in 1 CARTON / 15 mL in 1 JAR
Product Details
What is NDC 54111-152?
What are the uses for Naturopathica?
Which are Naturopathica UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Naturopathica 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)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- GALACTOARABINAN (UNII: SL4SX1O487)
- GLYCERIN (UNII: PDC6A3C0OX)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- DOCOSANOL (UNII: 9G1OE216XY)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- PROPANEDIOL (UNII: 5965N8W85T)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309)
- SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)
- ROSA DAMASCENA FLOWER OIL (UNII: 18920M3T13)
- TAGETES MINUTA FLOWER OIL (UNII: 1T0ZMU8M8B)
- CITRUS SINENSIS FLOWER OIL (UNII: AJ56JP5TFP)
- ETHYL FERULATE (UNII: 5B8915UELW)
- UNDARIA PINNATIFIDA (UNII: ICV1OK7M1S)
- POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- BORAGE SEED OIL (UNII: F8XAG1755S)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
- XYLITYLGLUCOSIDE (UNII: O0IEZ166FB)
- COCO GLUCOSIDE (UNII: ICS790225B)
- LEVOMENOL (UNII: 24WE03BX2T)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- ANHYDROXYLITOL (UNII: 8XWR7NN42F)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- XYLITOL (UNII: VCQ006KQ1E)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- POLYGONUM AVICULARE TOP (UNII: ZCD6009IUF)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- TREHALOSE (UNII: B8WCK70T7I)
- LUTEIN (UNII: X72A60C9MT)
* 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".