NDC 60432-834 Lindane
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 60432 - Morton Grove Pharmaceuticals, Inc.
- 60432-834 - Lindane
Product Characteristics
Product Packages
Product Details
What is NDC 60432-834?
What are the uses for Lindane?
Which are Lindane UNII Codes?
The UNII codes for the active ingredients in this product are:
- LINDANE (UNII: 59NEE7PCAB)
- LINDANE (UNII: 59NEE7PCAB) (Active Moiety)
Which are Lindane 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:
- ACETONE (UNII: 1364PS73AF)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- TROLAMINE LAURYL SULFATE (UNII: E8458C1KAA)
- WATER (UNII: 059QF0KO0R)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Lindane?
- RxCUI: 197878 - lindane 1 % Medicated Shampoo
- RxCUI: 197878 - lindane 10 MG/ML Medicated Shampoo
* Please review the disclaimer below.
Patient Education
Lindane
Lindane is used to treat scabies (mites that attach themselves to the skin) and lice (small insects that attach themselves to the skin on the head or pubic area ['crabs']). Lindane is in a class of medications called scabicides and pediculicides. It works by killing lice and mites. Lindane does not stop you from getting scabies or lice. You should only use lindane if you already have these conditions, not if you are afraid that you may get them.
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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".