ethyl rubbing alcohol
Generic: ethyl alcohol
Labeler: walgreen co.Drug Facts
Product Profile
Brand Name
ethyl rubbing alcohol
Generic Name
ethyl alcohol
Labeler
walgreen co.
Dosage Form
LIQUID
Routes
Active Ingredients
alcohol 70 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
0363-0876
Product ID
0363-0876_4a7d9069-39b4-00eb-e063-6394a90a8867
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M003
Listing Expiration
2027-12-31
Marketing Start
2009-05-18
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03630876
Hyphenated Format
0363-0876
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
ethyl rubbing alcohol (source: ndc)
Generic Name
ethyl alcohol (source: ndc)
Application Number
M003 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 70 mL/100mL
Packaging
- 473 mL in 1 BOTTLE, PLASTIC (0363-0876-43)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4a7d9069-39b4-00eb-e063-6394a90a8867", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["582753"], "spl_set_id": ["a08ef11f-5c4f-4821-a0c0-d6c89def0bea"], "manufacturer_name": ["Walgreen Co."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (0363-0876-43)", "package_ndc": "0363-0876-43", "marketing_start_date": "20090518"}], "brand_name": "Ethyl Rubbing Alcohol", "product_id": "0363-0876_4a7d9069-39b4-00eb-e063-6394a90a8867", "dosage_form": "LIQUID", "product_ndc": "0363-0876", "generic_name": "Ethyl Alcohol", "labeler_name": "Walgreen Co.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ethyl Rubbing Alcohol", "active_ingredients": [{"name": "ALCOHOL", "strength": "70 mL/100mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20090518", "listing_expiration_date": "20271231"}