rubbing
Generic: ethyl alcohol
Labeler: perrigo direct, incDrug Facts
Product Profile
Brand Name
rubbing
Generic Name
ethyl alcohol
Labeler
perrigo direct, inc
Dosage Form
LIQUID
Routes
Active Ingredients
alcohol 70 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
50804-876
Product ID
50804-876_4b316b7d-aee8-e5b3-e063-6294a90ab3f3
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
50804876
Hyphenated Format
50804-876
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
rubbing (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 (50804-876-43)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4b316b7d-aee8-e5b3-e063-6294a90ab3f3", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["582753"], "spl_set_id": ["ba2266d7-da25-495a-b035-97e149551c30"], "manufacturer_name": ["Perrigo Direct, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (50804-876-43)", "package_ndc": "50804-876-43", "marketing_start_date": "20090518"}], "brand_name": "Rubbing", "product_id": "50804-876_4b316b7d-aee8-e5b3-e063-6294a90ab3f3", "dosage_form": "LIQUID", "product_ndc": "50804-876", "generic_name": "Ethyl Alcohol", "labeler_name": "Perrigo Direct, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Rubbing", "active_ingredients": [{"name": "ALCOHOL", "strength": "70 mL/100mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20090518", "listing_expiration_date": "20271231"}