verucide wart remover kit
Generic: wart remover
Labeler: blaine labs inc.Drug Facts
Product Profile
Brand Name
verucide wart remover kit
Generic Name
wart remover
Labeler
blaine labs inc.
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
63347-720
Product ID
63347-720_8d1b445c-d868-4bc9-855a-785d3b33112e
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M028
Listing Expiration
2026-12-31
Marketing Start
2023-09-29
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63347720
Hyphenated Format
63347-720
Supplemental Identifiers
RxCUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
verucide wart remover kit (source: ndc)
Generic Name
wart remover (source: ndc)
Application Number
M028 (source: ndc)
Resolved Composition
Strengths
- 60 %
- 17 %
Packaging
- 1 KIT in 1 PACKAGE (63347-720-01) * 7.5 mL in 1 BOTTLE (63347-721-01) * 3 mL in 1 BOTTLE (63347-722-01)
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "8d1b445c-d868-4bc9-855a-785d3b33112e", "openfda": {"rxcui": ["312881", "1039483"], "spl_set_id": ["017f3ca2-6dba-4db5-b559-8ce0f2709772"], "manufacturer_name": ["Blaine Labs Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 PACKAGE (63347-720-01) * 7.5 mL in 1 BOTTLE (63347-721-01) * 3 mL in 1 BOTTLE (63347-722-01)", "package_ndc": "63347-720-01", "marketing_start_date": "20230929"}], "brand_name": "VERUCIDE WART REMOVER Kit", "product_id": "63347-720_8d1b445c-d868-4bc9-855a-785d3b33112e", "dosage_form": "KIT", "product_ndc": "63347-720", "generic_name": "Wart Remover", "labeler_name": "Blaine Labs Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "VERUCIDE WART REMOVER Kit", "application_number": "M028", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230929", "listing_expiration_date": "20261231"}