NDC 71055-100 Ice Sun Bc Air Puff
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Product Details
What is NDC 71055-100?
What are the uses for Ice Sun Bc Air Puff?
Which are Ice Sun Bc Air Puff UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Ice Sun Bc Air Puff 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:
- BUTANE (UNII: 6LV4FOR43R)
- PROPANE (UNII: T75W9911L6)
- WATER (UNII: 059QF0KO0R)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- PROPANEDIOL (UNII: 5965N8W85T)
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- C13-15 ALKANE (UNII: 114P5I43UJ)
- NIACINAMIDE (UNII: 25X51I8RD4)
- LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- HYDROGEN DIMETHICONE (13 CST) (UNII: 4QGR4P2YOI)
- TALC (UNII: 7SEV7J4R1U)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- ADENOSINE (UNII: K72T3FS567)
- HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- ALCOHOL (UNII: 3K9958V90M)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- ULTRAMARINE BLUE (UNII: I39WR998BI)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- GLYCERIN (UNII: PDC6A3C0OX)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- EPILOBIUM ANGUSTIFOLIUM FLOWERING TOP (UNII: 08H094218D)
- LILIUM LANCIFOLIUM BULB (UNII: 47Z05W73EZ)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAMELLIA JAPONICA FLOWER (UNII: KUB8101TNF)
- MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
- SAGE (UNII: 065C5D077J)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
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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".