isopropyl rubbing alcohol
Generic: isopropyl alcohol
Labeler: universal distribution center llcDrug Facts
Product Profile
Brand Name
isopropyl rubbing alcohol
Generic Name
isopropyl alcohol
Labeler
universal distribution center llc
Dosage Form
LIQUID
Routes
Active Ingredients
isopropyl alcohol 50 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
52000-801
Product ID
52000-801_2f982a20-e80a-a5a5-e063-6394a90a95f4
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M003
Listing Expiration
2026-12-31
Marketing Start
2012-06-29
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
52000801
Hyphenated Format
52000-801
Supplemental Identifiers
RxCUI
UPC
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
isopropyl rubbing alcohol (source: ndc)
Generic Name
isopropyl alcohol (source: ndc)
Application Number
M003 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mL/100mL
Packaging
- 355 mL in 1 BOTTLE, PLASTIC (52000-801-01)
- 946 mL in 1 BOTTLE, PLASTIC (52000-801-02)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2f982a20-e80a-a5a5-e063-6394a90a95f4", "openfda": {"upc": ["0676979556048"], "unii": ["ND2M416302"], "rxcui": ["616456"], "spl_set_id": ["2f982aef-4f46-aa85-e063-6394a90a52b1"], "manufacturer_name": ["Universal Distribution Center LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE, PLASTIC (52000-801-01)", "package_ndc": "52000-801-01", "marketing_start_date": "20120629"}, {"sample": false, "description": "946 mL in 1 BOTTLE, PLASTIC (52000-801-02)", "package_ndc": "52000-801-02", "marketing_start_date": "20120629"}], "brand_name": "Isopropyl Rubbing Alcohol", "product_id": "52000-801_2f982a20-e80a-a5a5-e063-6394a90a95f4", "dosage_form": "LIQUID", "product_ndc": "52000-801", "generic_name": "Isopropyl Alcohol", "labeler_name": "Universal Distribution Center LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Isopropyl Rubbing Alcohol", "active_ingredients": [{"name": "ISOPROPYL ALCOHOL", "strength": "50 mL/100mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120629", "listing_expiration_date": "20261231"}