NDC 69184-001 Super Bb All-in-1
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 69184-001?
What are the uses for Super Bb All-in-1?
Which are Super Bb All-in-1 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 Super Bb All-in-1 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:
- MICA (UNII: V8A1AW0880)
- BORON NITRIDE (UNII: 2U4T60A6YD)
- WATER (UNII: 059QF0KO0R)
- ZINC STEARATE (UNII: H92E6QA4FV)
- OCTYLDODECYL STEAROYL STEARATE (UNII: 3D47Q6D93C)
- LAUROYL LYSINE (UNII: 113171Q70B)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERIN (UNII: PDC6A3C0OX)
- TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- SALIX ALBA BARK (UNII: 205MXS71H7)
- BROWN IRON OXIDE (UNII: 1N032N7MFO)
- D&C RED NO. 6 (UNII: 481744AI4O)
- D&C RED NO. 7 (UNII: ECW0LZ41X8)
- ULTRAMARINE BLUE (UNII: I39WR998BI)
- FERRIC FERROCYANIDE (UNII: TLE294X33A)
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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".