NDC 54868-4730 Ortho Tri Cyclen Lo
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
BLUE (C48333 - LIGHT BLUE)
BLUE (C48333 - DARK BLUE)
GREEN (C48329 - DARK GREEN)
O;M;215
O;M;250
O;M;P
Code Structure Chart
Product Details
What is NDC 54868-4730?
What are the uses for Ortho Tri Cyclen Lo?
Which are Ortho Tri Cyclen Lo UNII Codes?
The UNII codes for the active ingredients in this product are:
- NORGESTIMATE (UNII: C291HFX4DY)
- NORGESTIMATE (UNII: C291HFX4DY) (Active Moiety)
- ETHINYL ESTRADIOL (UNII: 423D2T571U)
- ETHINYL ESTRADIOL (UNII: 423D2T571U) (Active Moiety)
Which are Ortho Tri Cyclen Lo 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:
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- WATER (UNII: 059QF0KO0R)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- STARCH, CORN (UNII: O8232NY3SJ)
- TALC (UNII: 7SEV7J4R1U)
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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".