NDC 69318-001 An12
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 69318-001?
What are the uses for An12?
Which are An12 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
Which are An12 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)
- HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16)
- SPANISH SARDINE (UNII: V837G5YR4R)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- COCO GLUCOSIDE (UNII: ICS790225B)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- CARICA PAPAYA LEAF (UNII: 66J7636Z2I)
- HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
- NEPIDERMIN (UNII: TZK30RF92W)
- RICE BRAN (UNII: R60QEP13IC)
- ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S)
- MUNG BEAN (UNII: 1LIB31N73G)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- PURSLANE (UNII: M6S840WXG5)
- RHEUM PALMATUM ROOT (UNII: G025DAL7CE)
- BAMBUSA VULGARIS TOP (UNII: FIW80T6P6V)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)
- MATRICARIA RECUTITA FLOWERING TOP (UNII: 3VNC7T6Z02)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
- OLEIC ACID (UNII: 2UMI9U37CP)
- PEG-60 CASTOR OIL (UNII: VXP26NM2XX)
- POMEGRANATE (UNII: 56687D1Z4D)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- MENTHOL (UNII: L7T10EIP3A)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
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[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".