NDC 52862-026 Isopropyl Rubbing Alcohol 99% With Wintergreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52862 - Home Smart Products
- 52862-026 - Isopropyl Rubbing Alcohol 99% With Wintergreen
Product Packages
NDC Code 52862-026-03
Package Description: 119 mL in 1 BOTTLE, PLASTIC
NDC Code 52862-026-04
Package Description: 178 mL in 1 BOTTLE, PLASTIC
NDC Code 52862-026-06
Package Description: 237 mL in 1 BOTTLE, PLASTIC
NDC Code 52862-026-09
Package Description: 295 mL in 1 BOTTLE, PLASTIC
NDC Code 52862-026-10
Package Description: 354 mL in 1 BOTTLE, PLASTIC
NDC Code 52862-026-11
Package Description: 414 mL in 1 BOTTLE, PLASTIC
NDC Code 52862-026-12
Package Description: 473 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 52862-026?
What are the uses for Isopropyl Rubbing Alcohol 99% With Wintergreen?
Which are Isopropyl Rubbing Alcohol 99% With Wintergreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)
Which are Isopropyl Rubbing Alcohol 99% With Wintergreen 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)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- PEG-75 LANOLIN (UNII: 09179OX7TB)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Isopropyl Rubbing Alcohol 99% With Wintergreen?
- RxCUI: 402481 - isopropyl alcohol 99 % Topical Solution
- RxCUI: 402481 - isopropyl alcohol 0.99 ML/ML Topical Solution
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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".