NDC 73006-111 Only For Sleep
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73006 - O4 Global Trading Usa, Llc
- 73006-111 - Only For
Product Characteristics
Product Packages
NDC Code 73006-111-41
Package Description: 1 BLISTER PACK in 1 CARTON / 4 TABLET in 1 BLISTER PACK
Product Details
What is NDC 73006-111?
What are the uses for Only For Sleep?
Which are Only For Sleep UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40)
- DIPHENHYDRAMINE (UNII: 8GTS82S83M) (Active Moiety)
Which are Only For Sleep 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:
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- D&C BLUE NO. 4 (UNII: 0KSY80VYS3)
- DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
- HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- MAGNESIUM PALMITOSTEARATE (UNII: R4OXA9G5BV)
- MICROCRYSTALLINE CELLULOSE 101 (UNII: 7T9FYH5QMK)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Only For Sleep?
- RxCUI: 1049630 - diphenhydrAMINE HCl 25 MG Oral Tablet
- RxCUI: 1049630 - diphenhydramine hydrochloride 25 MG Oral Tablet
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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".