NDC 43251-3333 Natralia Acne
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 43251-3333?
What are the uses for Natralia Acne?
Which are Natralia Acne UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) (Active Moiety)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- PULSATILLA VULGARIS (UNII: I76KB35JEV)
- PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
Which are Natralia Acne 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:
- CHAMOMILE (UNII: FGL3685T2X)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- LACTIC ACID (UNII: 33X04XA5AT)
- ZINC PIDOLATE (UNII: C32PQ86DH4)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- SORBITAN MONOPALMITATE (UNII: 77K6Z421KU)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SORBIC ACID (UNII: X045WJ989B)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SQUALANE (UNII: GW89575KF9)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ)
- TEA TREE OIL (UNII: VIF565UC2G)
- WITCH HAZEL (UNII: 101I4J0U34)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".