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American Safety First Aid Antispetic Hydrogen Peroxide 30 mL/1000mL Spray, 59.1 mL — NDC 71927-0013-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

American Safety First Aid Antispetic Hydrogen Peroxide 30 mL/1000mL Spray, 59.1 mL — NDC 71927-013-01 (Billing 71927-0013-01)

by Orazen Inc · 59.1 mL in 1 BOTTLE, SPRAY

This is a package of 59.1 mL of American Safety First Aid Antispetic Hydrogen Peroxide 30 mL/1000mL Spray from Orazen Inc, marketed since Oct 2022 and currently FDA-listed. It is this product's only package size.

NDC 71927-0013-01
🏷️ FDA NDC (as labeled) 71927-013-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

NDC database record

One package, one record: these facts belong to NDC 71927-013-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
71927 labeler · 013 product · 01 package
Package marketed since
Oct 3, 2022
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0747200606617
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 71927-013-01
Product NDC 71927-013
11-digit billing NDC 71927001301
RxCUI 283420
UNII BBX060AN9V
UPC 0747200606617
Application # M003
SPL Set ID ea2fbdfe-1932-9fb4-e053-2a95a90a3563
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2022-10-03
Route TOPICAL
Dosage form SPRAY
Substance HYDROGEN PEROXIDE
Quick answers
  • RxCUI (RxNorm): 283420
Why two NDCs? The FDA registers this code as 71927-013-01 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 71927-0013-01. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

RxNorm drug class

This medicine belongs to the Antiinfectives and antiseptics for local oral treatment class.

Drug family (ATC) Antiinfectives and antiseptics for local oral treatment, Other antiseptics and disinfectants, Other dermatologicals
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

Clinical

🧪 What is this product?

This is a spray bottle of hydrogen peroxide solution marketed as a first aid antiseptic for topical use on skin. Hydrogen peroxide is commonly used in over-the-counter antiseptic products to help cleanse minor cuts, scrapes, and wounds by releasing oxygen when it contacts damaged tissue. This product is regulated as an over-the-counter monograph drug, meaning it is marketed under established FDA guidelines for antiseptic ingredients rather than as an individually approved application.

Supplement & herbal interactions

Some supplements/herbs that may interact with Hydrogen Peroxide — tap one for details:

Dimethylsulfoxide (dmso)Moderate Turpentine OilModerate AlchemillaMinor
🌿 Every supplement checked against Hydrogen Peroxide (3 interactions) — ranked by severity →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer mLPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
71927-0013-01 You're viewing this Main listing 59.1 mL in 1 BOTTLE, SPRAY 2022-10-03 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
First Aid Only Hydrogen Peroxide 3% 30 mg/mL 00924-0935-01 Acme 59.1 ml — — FDA listed —
Hydrogen Peroxide 30 mg/mL 11344-0871-34 Nice-Pak 237 ml — — FDA listed —
Xpect Hydrogen Peroxide 3 mL/100mL 42961-0216-01 Cintas 59.1 ml — — FDA listed —
MediFirst Hydrogen Peroxide 43.275 g/L 47682-0257-02 Unifirst 0591 l — — FDA listed —
Hydrogen Peroxide 30 mL/L 47682-0304-02 Unifirst 0591 l — — FDA listed —
Green Guard Hydrogen Peroxide 30 mL/L 47682-0324-02 Unifirst 0591 l — — FDA listed —
Green Guard Hydrogen Peroxide 30 mL/L 47682-0334-02 Unifirst 0591 l — — FDA listed —
Hydrogen Peroxide 30 mg/mL 50332-0219-02 HART 60 ml — — FDA listed —
Hydrogen Peroxide 30 mg/mL 50332-0229-02 HART 60 ml — — FDA listed —
Hydrogen Peroxide 30 mg/mL 50804-0871-34 Perrigo 236 ml — — FDA listed —
American Red Cross 6oz, 3% Hydrogen Peroxide 5.31 mL/177mL 51628-3775-01 MY 177 ml — — FDA listed —
American Red Cross 3 Hydrogen Peroxide 30 mg/mL 51628-4238-01 MY 177 ml — — FDA listed —
Water Jel Hydrogen Peroxide 3 mL/100mL 59898-0403-10 Water-Jel 59 ml — — FDA listed —
Hydrogen Peroxide 30 mg/mL 61010-5400-02 Safetec 59.1 ml — — FDA listed —
Hydrogen Peroxide 30 mL/L 69396-0108-02 Trifecta 059 l — — FDA listed —
American Safety First Aid Antispetic 30 mL/1000mLthis 71927-0013-01 Orazen 59.1 ml — — FDA listed —
Hydrogen Peroxide 30 mg/mL 73598-0661-01 JHK 59.1 ml — — FDA listed —
MEDI-FIRST First Aid Antiseptic 30 mL/L 78495-0162-01 Ultra 0591 l — — FDA listed —
Biopure 3 Hydrogen Peroxide 30 mg/mL 78691-0021-50 Quest 177 ml — — FDA listed —
Hydrogen Peroxide 30 mg/mL 84269-3503-01 Wildman 59.1 ml — — FDA listed —
Oopsie 3 Hydrogen Peroxide 30 mg/mL 87251-0006-06 4 177 ml — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2022
On the market since
Oct 2022
📍
2026
Currently FDA-listed
4 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

1 inactive ingredient listed in the exact product block matched to this NDC.

The official label also stateswater

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerOrazen Inc
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code71927
First marketedOct 2022
Product typeHuman Otc Drug
Portfolio25 products on file

More NDCs from Orazen Inc labeler code 71927

The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 Ask a Doctor Before Use If 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 13 words ▾

Uses first aid to help prevent infection in minor cuts, scrapes and burns

⏱️ Dosage and Administration 32 words ▾

Directions clean the affected area spray a small amount of this product on the area 1 to 3 times daily may be covered with a sterile bandage if bandaged, let dry first

⚠️ Warnings 5 words ▾

Warnings For external use only

🧪 Active Ingredient 5 words ▾

Active ingredient Hydrogen peroxide 3%

🧪 Inactive Ingredients 3 words ▾

Inactive ingredients water

🎯 Purpose 4 words ▾

Purpose First aid antiseptic

📄 Do Not Use 23 words ▾

Do not use in the eyes or apply over large areas of the body longer than 1 week unless directed by a doctor

📄 Ask a Doctor Before Use If 17 words ▾

Ask a doctor before use if you have deep or puncture wounds, animal bites, or serious burns

📄 Stop Use and Ask a Doctor If 13 words ▾

Stop use and ask a doctor if the condition persists or gets worse

📄 Keep Out of Reach of Children 19 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📄 Other Information 6 words ▾

Other information store at room temperature

📄 Questions or Comments 5 words ▾

Questions? 1-866-651-3660 Mon-Fri 8:00am-5:00pm EST

📄 Package Label / Principal Display Panel 10 words ▾

Package Label - Principal Display Panel image of bottle label

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for American Safety First Aid Antispetic (this brand).

Top reported reactions

Pemphigus1,529
Glossodynia1,528
Hand Deformity1,508
Joint Swelling1,508
Helicobacter Infection1,501
Impaired Healing1,495
Infusion Related Reaction1,495

Age at onset

Neonate25
Child2
Adolescent3
Adult640
Elderly40

Reporter sex

3,842 reports
Male · 6%
Female · 94%
Unknown · 0%

Serious outcomes

Disabling2,646
Hospitalization2,536
Life-threatening2,496
Death2,370
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 1,343 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

About this NDC listing & data coverage

Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Orazen Inc. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Orazen Inc is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
← 71927-0012-01 · Orazen 71927-0014-01 · Orazen →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.