benzoin compound tincture
Generic: benzoin resin
Labeler: humco holding group, inc.Drug Facts
Product Profile
Brand Name
benzoin compound tincture
Generic Name
benzoin resin
Labeler
humco holding group, inc.
Dosage Form
LIQUID
Routes
Active Ingredients
benzoin resin 1000 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0395-0243
Product ID
0395-0243_45b3d3ef-3410-79a1-e063-6394a90a758d
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M022
Listing Expiration
2026-12-31
Marketing Start
2008-01-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03950243
Hyphenated Format
0395-0243
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
benzoin compound tincture (source: ndc)
Generic Name
benzoin resin (source: ndc)
Application Number
M022 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1000 mg/mL
Packaging
- 473 mL in 1 BOTTLE, PLASTIC (0395-0243-16)
- 59 mL in 1 BOTTLE, PLASTIC (0395-0243-92)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "45b3d3ef-3410-79a1-e063-6394a90a758d", "openfda": {"upc": ["0303950243160", "0303950243924"], "unii": ["GK21SBA74R"], "spl_set_id": ["a893a232-2ea8-4e0d-8cbf-7f5040b3be2e"], "manufacturer_name": ["Humco Holding Group, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (0395-0243-16)", "package_ndc": "0395-0243-16", "marketing_start_date": "20171110"}, {"sample": false, "description": "59 mL in 1 BOTTLE, PLASTIC (0395-0243-92)", "package_ndc": "0395-0243-92", "marketing_start_date": "20171110"}], "brand_name": "Benzoin Compound Tincture", "product_id": "0395-0243_45b3d3ef-3410-79a1-e063-6394a90a758d", "dosage_form": "LIQUID", "product_ndc": "0395-0243", "generic_name": "Benzoin Resin", "labeler_name": "Humco Holding Group, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Benzoin Compound Tincture", "active_ingredients": [{"name": "BENZOIN RESIN", "strength": "1000 mg/mL"}], "application_number": "M022", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20080101", "listing_expiration_date": "20261231"}