hydrogen peroxide
Generic: hydrogen peroxide
Labeler: o&m halyard, inc.Drug Facts
Product Profile
Brand Name
hydrogen peroxide
Generic Name
hydrogen peroxide
Labeler
o&m halyard, inc.
Dosage Form
LIQUID
Routes
Active Ingredients
hydrogen peroxide 30 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
39892-0710
Product ID
39892-0710_40b23cd3-833c-28e9-e063-6394a90ae212
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M003
Listing Expiration
2026-12-31
Marketing Start
2019-03-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
398920710
Hyphenated Format
39892-0710
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
hydrogen peroxide (source: ndc)
Generic Name
hydrogen peroxide (source: ndc)
Application Number
M003 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/mL
Packaging
- 30 mL in 1 PACKET (39892-0710-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "40b23cd3-833c-28e9-e063-6394a90ae212", "openfda": {"unii": ["BBX060AN9V"], "rxcui": ["91349"], "spl_set_id": ["0ad5990a-a18d-4753-826b-6da313926698"], "manufacturer_name": ["O&M HALYARD, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 PACKET (39892-0710-1)", "package_ndc": "39892-0710-1", "marketing_start_date": "20190301"}], "brand_name": "Hydrogen Peroxide", "product_id": "39892-0710_40b23cd3-833c-28e9-e063-6394a90ae212", "dosage_form": "LIQUID", "product_ndc": "39892-0710", "generic_name": "HYDROGEN PEROXIDE", "labeler_name": "O&M HALYARD, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Hydrogen Peroxide", "active_ingredients": [{"name": "HYDROGEN PEROXIDE", "strength": "30 mg/mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190301", "listing_expiration_date": "20261231"}