NDC 70648-133 Olp Anti-itch Allergy Relief

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
70648-133
Proprietary Name:
Olp Anti-itch Allergy Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ohio Lab Pharma Llc.
Labeler Code:
70648
Start Marketing Date: [9]
02-21-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

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?

The NDC code 70648-133 is assigned by the FDA to the product Olp Anti-itch Allergy Relief which is product labeled by Ohio Lab Pharma Llc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70648-133-01 1 tube in 1 carton / 20 g in 1 tube. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Olp Anti-itch Allergy Relief?

Do not use more than directedadults and children 2 years of age and older: apply to affected area not more than 3 to 4 times dailychildren under 2 years of age: ask a doctor

Which are Olp Anti-itch Allergy Relief UNII Codes?

The UNII codes for the active ingredients in this product are:

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:

What is the NDC to RxNorm Crosswalk for Olp Anti-itch Allergy Relief?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • 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

* Please review the disclaimer below.

Product Footnotes

[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".