NDC 70648-999 Olp Baby Teething
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70648 - Ohio Lab Pharma
- 70648-999 - Olp Baby Teething
Product Characteristics
Product Packages
NDC Code 70648-999-01
Package Description: 1 TUBE in 1 CARTON / 9.4 g in 1 TUBE
Product Details
What is NDC 70648-999?
What are the uses for Olp Baby Teething?
Which are Olp Baby Teething UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
Which are Olp Baby Teething 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)
- SORBIC ACID (UNII: X045WJ989B)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- CARBOMER 980 (UNII: 4Q93RCW27E)
- SORBITOL (UNII: 506T60A25R)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
What is the NDC to RxNorm Crosswalk for Olp Baby Teething?
- RxCUI: 198496 - benzocaine 7.5 % Oral Gel
- RxCUI: 198496 - benzocaine 0.075 MG/MG Oral Gel
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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".