NDC 70648-133 Olp Anti-itch Allergy Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70648 - Ohio Lab Pharma Llc.
- 70648-133 - Olp Anti-itch Allergy Relief
Product Characteristics
Product Packages
NDC Code 70648-133-01
Package Description: 1 TUBE in 1 CARTON / 20 g in 1 TUBE
Product Details
What is NDC 70648-133?
What are the uses for Olp Anti-itch Allergy Relief?
Which are Olp Anti-itch Allergy Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40)
- DIPHENHYDRAMINE (UNII: 8GTS82S83M) (Active Moiety)
- ZINC ACETATE (UNII: FM5526K07A)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Olp Anti-itch Allergy Relief 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)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- DECYL OLEATE (UNII: ZGR06DO97T)
- SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B)
- TROLAMINE (UNII: 9O3K93S3TK)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- EDETIC ACID (UNII: 9G34HU7RV0)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
What is the NDC to RxNorm Crosswalk for Olp Anti-itch Allergy Relief?
- RxCUI: 1292313 - diphenhydrAMINE HCl 1 % / zinc acetate 0.1 % Topical Cream
- RxCUI: 1292313 - diphenhydramine hydrochloride 10 MG/ML / zinc acetate 1 MG/ML Topical Cream
- RxCUI: 1292313 - diphenhydramine hydrochloride 1 % / zinc acetate 0.1 % Topical Cream
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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".