hydrogen peroxide
Generic: hydrogen peroxide
Labeler: jhk incDrug Facts
Product Profile
Brand Name
hydrogen peroxide
Generic Name
hydrogen peroxide
Labeler
jhk inc
Dosage Form
SPRAY
Routes
Active Ingredients
hydrogen peroxide 30 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
73598-0661
Product ID
73598-0661_761a3a3d-c052-47b3-a86b-bf07bf5fde9b
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M004
Listing Expiration
2026-12-31
Marketing Start
2020-02-14
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
735980661
Hyphenated Format
73598-0661
Supplemental Identifiers
RxCUI
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
hydrogen peroxide (source: ndc)
Generic Name
hydrogen peroxide (source: ndc)
Application Number
M004 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/mL
Packaging
- 59.1 mL in 1 BOTTLE, SPRAY (73598-0661-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "761a3a3d-c052-47b3-a86b-bf07bf5fde9b", "openfda": {"upc": ["0747200606617"], "unii": ["BBX060AN9V"], "rxcui": ["283420"], "spl_set_id": ["1472c854-09c8-4ad8-b8a6-0235440ac26b"], "manufacturer_name": ["JHK Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59.1 mL in 1 BOTTLE, SPRAY (73598-0661-1)", "package_ndc": "73598-0661-1", "marketing_start_date": "20200214"}], "brand_name": "Hydrogen Peroxide", "product_id": "73598-0661_761a3a3d-c052-47b3-a86b-bf07bf5fde9b", "dosage_form": "SPRAY", "product_ndc": "73598-0661", "generic_name": "Hydrogen Peroxide", "labeler_name": "JHK Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Hydrogen Peroxide", "active_ingredients": [{"name": "HYDROGEN PEROXIDE", "strength": "30 mg/mL"}], "application_number": "M004", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200214", "listing_expiration_date": "20261231"}