Tucks Multi-care Relief Kit (tucks Hemorrhoidal And Tucks Medicated Cooling 40 Count) Kit
NDC Package 10157-2112-1
Package Information
Tucks Multi-care Relief Kit (tucks Hemorrhoidal And Tucks Medicated Cooling 40 Count) (glycerin, lidocaine, and witch hazel) kits is adults:when practical, clean the affected area with mild soap and warm water and rinse thoroughlygently dry by patting or blotting with toilet tissue or a soft cloth before applyingapply externally to the affected area up to 6 times daily or after each bowel movementChildren under 12 years of age: ask a doctor Adults:when practical, clean the affected area with mild soap and warm water and rinse thoroughlygently dry by patting or blotting with toilet tissue or a soft cloth before applyingapply externally to the affected area up to 6 times daily or after each bowel movementafter application, discard pad and wash handsChildren under 12 years of age: ask a doctor. This formulation utilizes a kit delivery system. Marketed by Blistex Inc, this product is identified by NDC 10157-2112 and is authorized under FDA application M015.
Identification & Billing
- RxCUI: 2117860 - glycerin 15 % / lidocaine 5 % Topical Hemorrhoidal Cream
- RxCUI: 2117860 - glycerin 150 MG/ML / lidocaine 50 MG/ML Topical Cream
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 10157 - Blistex Inc
- 10157-2112 - Tucks Multi-care Relief Kit (tucks Hemorrhoidal And Tucks Medicated Cooling 40 Count)
- 10157-2112-1 - 1 KIT in 1 CARTON * 1 mL in 1 APPLICATOR * 14 g in 1 TUBE
- 10157-2112 - Tucks Multi-care Relief Kit (tucks Hemorrhoidal And Tucks Medicated Cooling 40 Count)
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 10157-2112-1 identifies a specific commercial package of 1 kit in 1 carton * 1 ml in 1 applicator * 14 g in 1 tube of Tucks Multi-care Relief Kit (tucks Hemorrhoidal And Tucks Medicated Cooling 40 Count), a human over the counter drug labeled by Blistex Inc. This kit is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Blistex Inc on February 15, 2019. The current certification is valid through December 31, 2026.
How is this Blistex Inc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 10157211201. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.