de la cruz decolorized iodine
Generic: ethyl alcohol
Labeler: dlc laboratories, inc.Drug Facts
Product Profile
Brand Name
de la cruz decolorized iodine
Generic Name
ethyl alcohol
Labeler
dlc laboratories, inc.
Dosage Form
LIQUID
Routes
Active Ingredients
alcohol .45 mL/mL
Manufacturer
Identifiers & Regulatory
Product NDC
24286-1529
Product ID
24286-1529_299414ed-41eb-0dbb-e063-6394a90a88f9
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M003
Listing Expiration
2026-12-31
Marketing Start
1998-03-25
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
242861529
Hyphenated Format
24286-1529
Supplemental Identifiers
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
de la cruz decolorized iodine (source: ndc)
Generic Name
ethyl alcohol (source: ndc)
Application Number
M003 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .45 mL/mL
Packaging
- 59 mL in 1 BOTTLE, PLASTIC (24286-1529-8)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "299414ed-41eb-0dbb-e063-6394a90a88f9", "openfda": {"upc": ["0324286153220"], "unii": ["3K9958V90M"], "spl_set_id": ["5d8f6aaa-0b87-1166-e053-2991aa0a297f"], "manufacturer_name": ["DLC Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59 mL in 1 BOTTLE, PLASTIC (24286-1529-8)", "package_ndc": "24286-1529-8", "marketing_start_date": "20171106"}], "brand_name": "De La Cruz Decolorized Iodine", "product_id": "24286-1529_299414ed-41eb-0dbb-e063-6394a90a88f9", "dosage_form": "LIQUID", "product_ndc": "24286-1529", "generic_name": "Ethyl Alcohol", "labeler_name": "DLC Laboratories, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "De La Cruz Decolorized Iodine", "active_ingredients": [{"name": "ALCOHOL", "strength": ".45 mL/mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19980325", "listing_expiration_date": "20261231"}