Home NDC 60635-018 NDC 60635-018 - Varithena This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 60635-018
Package NDCs from labels 60635-018-01
Manufacturer Boston Scientific Corporation | Boston Scientific Limited (Ireland) Cork
Effective date 2026-10-07
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 60635-018-01 Varithena 18 mL in 1 CANISTER INJECTABLE FOAM 18 mL 10 mg in 1mL 17 60635-018-01 Varithena 18 mL in 1 CANISTER INJECTABLE FOAM 18 mL 10 mg in 1mL 17 60635-018-01 Varithena 18 mL in 1 CANISTER INJECTABLE FOAM 18 mL 10 mg in 1mL 17
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 60635-018 VARITHENA (POLIDOCANOL) KIT [BIOCOMPATIBLES, INC.] 14 Unmatched 20241012_dfd6b4a0-b0dc-11e2-9e96-0800200c9a66.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded POLIDOCANOL ACTIVE INGREDIENT 0AWH8BFG9A VARITHENA (POLIDOCANOL) KIT [BIOCOMPATIBLES, INC.] 5 POLIDOCANOL ACTIVE MOIETY 0AWH8BFG9A VARITHENA (POLIDOCANOL) KIT [BIOCOMPATIBLES, INC.] 5 ALCOHOL INACTIVE INGREDIENT 3K9958V90M VARITHENA (POLIDOCANOL) KIT [BIOCOMPATIBLES, INC.] 5 CARBON DIOXIDE INACTIVE INGREDIENT 142M471B3J VARITHENA (POLIDOCANOL) KIT [BIOCOMPATIBLES, INC.] 5 OXYGEN INACTIVE INGREDIENT S88TT14065 VARITHENA (POLIDOCANOL) KIT [BIOCOMPATIBLES, INC.] 5 POTASSIUM PHOSPHATE, MONOBASIC INACTIVE INGREDIENT 4J9FJ0HL51 VARITHENA (POLIDOCANOL) KIT [BIOCOMPATIBLES, INC.] 5 SODIUM PHOSPHATE, DIBASIC, DIHYDRATE INACTIVE INGREDIENT 94255I6E2T VARITHENA (POLIDOCANOL) KIT [BIOCOMPATIBLES, INC.] 5 WATER INACTIVE INGREDIENT 059QF0KO0R VARITHENA (POLIDOCANOL) KIT [BIOCOMPATIBLES, INC.] 5
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 134 of 177 · 3,534 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Anti Bacterial Hand Gel Frozen Lake ALCOHOL Bath & Body Works, Inc. 29a536d5-6abb-c0ef-e063-6394a90a15bb 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Marshmallow Pumpkin Latte ALCOHOL Bath & Body Works, Inc. 29a5342a-e6dc-ea55-e063-6394a90a11e8 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pumpkin Apple ALCOHOL Bath & Body Works, Inc. 29a536d5-6abf-c0ef-e063-6394a90a15bb 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Fresh Rainfall ALCOHOL Bath & Body Works, Inc. 29a54361-e107-20d7-e063-6294a90a117a 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pumpkin Cupcake ALCOHOL Bath & Body Works, Inc. 29a53c91-0bda-f572-e063-6294a90ae895 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Sweater Weather ALCOHOL Bath & Body Works, Inc. 29a540fd-60b7-eb1e-e063-6394a90a27f7 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Alcohol Antiseptic 70% Topical Solution ALCOHOL Mycone Dental Supply Co., Inc DBA Keystone Industries and Deepak Products Inc aa95e99f-5c17-c394-e053-2995a90a6bf9 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Thick Hand Sanitizer ALCOHOL Mycone Dental Supply Co., Inc DBA Keystone Industries and Deepak Products Inc a35b4c26-469b-72ec-e053-2a95a90a0510 2024-12-19 Warnings Exact identifier unii: 3K9958V90M germstarONE unscented ETHYL ALCOHOL Soaptronic, LLC a6a798bd-09cb-1853-e053-2995a90a27f9 2024-12-19 Warnings Exact identifier unii: 3K9958V90M EXTENDED CARE Foaming Hand Sanitizer ALCOHOL TRIPLE A SUPPLIES, INC. f244f9c0-82c6-42a8-b0a8-63af546ed26f 2024-12-19 Warnings Exact identifier unii: 3K9958V90M germstarCitrus ETHYL ALCOHOL Soaptronic, LLC 779abef7-53ff-47c3-b7e6-27570eb055b3 2024-12-19 Warnings Exact identifier unii: 3K9958V90M germstarGel ETHYL ALCOHOL Soaptronic, LLC b5fd6c3c-d452-74e6-e053-2995a90a9090 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Cucumber Melon ALCOHOL Bath & Body Works, Inc. 29a63c54-116f-30bb-e063-6394a90a8c6f 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Frosted Coconut Snowball ALCOHOL Bath & Body Works, Inc. 29a652a8-15fd-80d4-e063-6394a90acb4d 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Black Cherry Frost ALCOHOL Bath & Body Works, Inc. 29a654df-016b-830e-e063-6394a90a1062 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Winterberry Ice ALCOHOL Bath & Body Works, Inc. 29a64c95-eb54-8081-e063-6394a90a0726 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Magic In The Air ALCOHOL Bath & Body Works, Inc. 29a651e4-a014-57d2-e063-6394a90a35f0 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Sweet Tea and Lemonade ALCOHOL Bath & Body Works, Inc. 29a64de5-af39-5a91-e063-6394a90ac35c 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Honolulu Sun ALCOHOL Bath & Body Works, Inc. 29a64c62-8517-1b39-e063-6294a90a35a8 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Strawberry Snowflakes ALCOHOL Bath & Body Works, Inc. 29a651e4-a016-57d2-e063-6394a90a35f0 2024-12-19 Warnings Exact identifier unii: 3K9958V90M
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.