benzoin tincture

Generic: benzoin resin

Labeler: pharma nobis, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name benzoin tincture
Generic Name benzoin resin
Labeler pharma nobis, llc
Dosage Form LIQUID
Routes
TOPICAL
Active Ingredients

benzoin resin 1000 mg/mL

Manufacturer
Pharma Nobis, LLC

Identifiers & Regulatory

Product NDC 82645-924
Product ID 82645-924_0d6cc91d-1d9b-25ae-e063-6394a90aa6a0
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 82645924
Hyphenated Format 82645-924

Supplemental Identifiers

UNII
GK21SBA74R

Packaging Origin

Original Packager
true

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 tincture (source: ndc)
Generic Name benzoin resin (source: ndc)
Application Number M022 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/mL
source: ndc
Packaging
  • 59 mL in 1 BOTTLE, PLASTIC (82645-924-92)
source: ndc

Packages (1)

82645-924-92 59 mL in 1 BOTTLE, PLASTIC (82645-924-92)

Ingredients (1)

benzoin resin (1000 mg/mL)

Linked Drug Pages (1)

Benzoin Tincture ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "0d6cc91d-1d9b-25ae-e063-6394a90aa6a0", "openfda": {"unii": ["GK21SBA74R"], "spl_set_id": ["e42fccc2-1b4f-e7f3-e053-2a95a90aef39"], "manufacturer_name": ["Pharma Nobis, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59 mL in 1 BOTTLE, PLASTIC (82645-924-92)", "package_ndc": "82645-924-92", "marketing_start_date": "20171212"}], "brand_name": "Benzoin Tincture", "product_id": "82645-924_0d6cc91d-1d9b-25ae-e063-6394a90aa6a0", "dosage_form": "LIQUID", "product_ndc": "82645-924", "generic_name": "Benzoin Resin", "labeler_name": "Pharma Nobis, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Benzoin 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"}