50% isopropyl alcohol
Generic: isopropyl alcohol
Labeler: h e bDrug Facts
Product Profile
Brand Name
50% isopropyl alcohol
Generic Name
isopropyl alcohol
Labeler
h e b
Dosage Form
SOLUTION
Routes
Active Ingredients
isopropyl alcohol 50 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
59640-864
Product ID
59640-864_4b9432b9-f8d8-7f15-e063-6394a90a9b64
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M003
Listing Expiration
2027-12-31
Marketing Start
2018-05-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59640864
Hyphenated Format
59640-864
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
50% isopropyl alcohol (source: ndc)
Generic Name
isopropyl alcohol (source: ndc)
Application Number
M003 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mL/100mL
Packaging
- 473 mL in 1 BOTTLE, PLASTIC (59640-864-43)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4b9432b9-f8d8-7f15-e063-6394a90a9b64", "openfda": {"unii": ["ND2M416302"], "rxcui": ["616456"], "spl_set_id": ["0ed762dd-9432-45b4-9e75-c24fb28ff956"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (59640-864-43)", "package_ndc": "59640-864-43", "marketing_start_date": "20180501"}], "brand_name": "50% Isopropyl Alcohol", "product_id": "59640-864_4b9432b9-f8d8-7f15-e063-6394a90a9b64", "dosage_form": "SOLUTION", "product_ndc": "59640-864", "generic_name": "Isopropyl Alcohol", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "50% Isopropyl Alcohol", "active_ingredients": [{"name": "ISOPROPYL ALCOHOL", "strength": "50 mL/100mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180501", "listing_expiration_date": "20271231"}