70 rubbing ethyl alcohol
Generic: alcohol
Labeler: iron lab sa de cvDrug Facts
Product Profile
Brand Name
70 rubbing ethyl alcohol
Generic Name
alcohol
Labeler
iron lab sa de cv
Dosage Form
LIQUID
Routes
Active Ingredients
alcohol 70 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
74375-050
Product ID
74375-050_4b08cc0e-f67a-9080-e063-6294a90a46af
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M003
Listing Expiration
2027-12-31
Marketing Start
2025-04-07
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
74375050
Hyphenated Format
74375-050
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
70 rubbing ethyl alcohol (source: ndc)
Generic Name
alcohol (source: ndc)
Application Number
M003 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 70 mL/100mL
Packaging
- 355 mL in 1 BOTTLE, DROPPER (74375-050-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4b08cc0e-f67a-9080-e063-6294a90a46af", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["1041849"], "spl_set_id": ["323be8b4-4588-e2a6-e063-6394a90ab68b"], "manufacturer_name": ["Iron Lab SA de CV"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE, DROPPER (74375-050-01)", "package_ndc": "74375-050-01", "marketing_start_date": "20250407"}], "brand_name": "70 Rubbing Ethyl Alcohol", "product_id": "74375-050_4b08cc0e-f67a-9080-e063-6294a90a46af", "dosage_form": "LIQUID", "product_ndc": "74375-050", "generic_name": "Alcohol", "labeler_name": "Iron Lab SA de CV", "product_type": "HUMAN OTC DRUG", "brand_name_base": "70 Rubbing Ethyl Alcohol", "active_ingredients": [{"name": "ALCOHOL", "strength": "70 mL/100mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250407", "listing_expiration_date": "20271231"}