NDC 49520-101 Obliterate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49520 - Mybody
- 49520-101 - Obliterate
Product Packages
NDC Code 49520-101-51
Package Description: 1 BOTTLE in 1 BOX / 15 mL in 1 BOTTLE (49520-101-11)
Product Details
What is NDC 49520-101?
What are the uses for Obliterate?
Which are Obliterate UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM)
- BENZOIC ACID (UNII: 8SKN0B0MIM) (Active Moiety)
Which are Obliterate 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)
- POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- ACETYL CARBOXYMETHYL COCOYL GLYCINE (UNII: 3TNX4P92J3)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- DECYLENE GLYCOL (UNII: S57M60MI88)
- CARBOMER HOMOPOLYMER (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)
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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".