NDC 0436-0669 Di-dak-sol
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What is NDC 0436-0669?
What are the uses for Di-dak-sol?
Which are Di-dak-sol UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM HYPOCHLORITE (UNII: DY38VHM5OD)
- HYPOCHLOROUS ACID (UNII: 712K4CDC10) (Active Moiety)
Which are Di-dak-sol 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:
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Di-dak-sol?
- RxCUI: 665046 - sodium hypochlorite 0.0125 % Topical Solution
- RxCUI: 665046 - sodium hypochlorite 0.125 MG/ML Topical Solution
- RxCUI: 979137 - DI-DAK-SOL 0.0125 % Topical Solution
- RxCUI: 979137 - sodium hypochlorite 0.125 MG/ML Topical Solution [Di-Dak-Sol]
- RxCUI: 979137 - Di-Dak-Sol 0.0125 % 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".