alcoh-wipe
Generic: isopropyl alcohol
Labeler: veltek associates, inc.Drug Facts
Product Profile
Brand Name
alcoh-wipe
Generic Name
isopropyl alcohol
Labeler
veltek associates, inc.
Dosage Form
SWAB
Routes
Active Ingredients
isopropyl alcohol .7 mL/mL
Manufacturer
Identifiers & Regulatory
Product NDC
64307-002
Product ID
64307-002_459ea895-979a-b547-e063-6294a90a3443
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2025-11-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
64307002
Hyphenated Format
64307-002
Supplemental Identifiers
RxCUI
UNII
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
alcoh-wipe (source: ndc)
Generic Name
isopropyl alcohol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .7 mL/mL
Packaging
- 1.03 mL in 1 PACKET (64307-002-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "459ea895-979a-b547-e063-6294a90a3443", "openfda": {"unii": ["ND2M416302"], "rxcui": ["797544"], "spl_set_id": ["343ba13e-7f90-5dab-e063-6294a90a56ae"], "manufacturer_name": ["Veltek Associates, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1.03 mL in 1 PACKET (64307-002-01)", "package_ndc": "64307-002-01", "marketing_start_date": "20251101"}], "brand_name": "ALCOH-WIPE", "product_id": "64307-002_459ea895-979a-b547-e063-6294a90a3443", "dosage_form": "SWAB", "product_ndc": "64307-002", "generic_name": "Isopropyl alcohol", "labeler_name": "Veltek Associates, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ALCOH-WIPE", "active_ingredients": [{"name": "ISOPROPYL ALCOHOL", "strength": ".7 mL/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251101", "listing_expiration_date": "20261231"}