NDC 42783-323 Ultrasal-er
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42783 - Elorac, Inc.
- 42783-323 - Ultrasal-er
Product Packages
NDC Code 42783-323-10
Package Description: 1 BOTTLE, WITH APPLICATOR in 1 CARTON / 10 mL in 1 BOTTLE, WITH APPLICATOR
Product Details
What is NDC 42783-323?
What are the uses for Ultrasal-er?
Which are Ultrasal-er UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Ultrasal-er?
- RxCUI: 1487371 - salicylic acid 28.5 % Topical Solution
- RxCUI: 1487371 - salicylic acid 285 MG/ML Topical Solution
- RxCUI: 1487376 - UltraSal-ER 28.5 % Wart Remover Topical Solution
- RxCUI: 1487376 - salicylic acid 285 MG/ML Topical Solution [Ultrasal]
- RxCUI: 1487376 - Ultrasal 285 MG/ML Topical Solution
* Please review the disclaimer below.
Patient Education
Salicylic Acid Topical
Topical salicylic acid is used to help clear and prevent pimples and skin blemishes in people who have acne. Topical salicylic acid is also used to treat skin conditions that involve scaling or overgrowth of skin cells such as psoriasis (a skin disease in which red, scaly patches form on some areas of the body), ichthyoses (inborn conditions that cause skin dryness and scaling), dandruff, corns, calluses, and warts on the hands or feet. Topical salicylic acid should not be used to treat genital warts, warts on the face, warts with hair growing from them, warts in the nose or mouth, moles, or birthmarks. Salicylic acid is in a class of medications called keratolytic agents. Topical salicylic acid treats acne by reducing swelling and redness and unplugging blocked skin pores to allow pimples to shrink. It treats other skin conditions by softening and loosening dry, scaly, or thickened skin so that it falls off or can be removed easily.
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* Please review the disclaimer below.
[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".