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Smelling Salt Ammonium Carbonate 4.5 g/30g Liquid, 30 g — NDC 85999-0001-01 package photo

Smelling Salt Ammonium Carbonate 4.5 g/30g Liquid, 30 g

by Nanning Xingshuang Network Technology Studio (A Sole Proprietorship) · 30 g in 1 BOTTLE (85999-001-01)
NDC 85999-0001-01
🏷️ FDA NDC (as labeled) 85999-001-01 billing pads the product segment with a zero
OTC Discontinued Non-controlled ⚠ Inactivated by FDA
🗂️ Data synced 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

⚠️
Excluded from the active FDA NDC Directory. FDA inactivated this product’s listing record, so it is excluded from the active NDC Directory. The listing was last certified through Dec 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

🆔 Identity & classification

FDA NDC (as labeled) 85999-001-01
Product NDC 85999-001
11-digit billing NDC 85999000101
RxCUI 1299889
UNII NJ5VT0FKLJ
Application # M011
SPL Set ID 3bbdb3a8-d0a9-cb90-e063-6394a90a41e0
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Inactivated by FDA (certified through Dec 2026)
Marketing start 2025-08-07
Route RESPIRATORY (INHALATION)
Dosage form LIQUID
Substance AMMONIUM CARBONATE
Why two NDCs? The FDA registers this code as 85999-001-01 — 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 → 85999-0001-01. 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 Radioactive Diagnostic Agent class.

Pharmacologic class Radioactive Diagnostic Agent
Drug family (ATC) Other cardiovascular system diagnostic radiopharmaceuticals
How it works Radiopharmaceutical Activity
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.

🏭 Manufacturer & labeler

LabelerNanning Xingshuang Network Technology Studio (A Sole Proprietorship)
FDA applicationM011 (OTC MONOGRAPH DRUG)
Labeler code85999
First marketedAug 2025
Product typeHuman Otc Drug
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.

🩺 Clinical

🧪 What is this product?

This is an over-the-counter inhalant product containing ammonium carbonate as its active ingredient. Ammonium carbonate is a volatile compound that is typically inhaled briefly to stimulate respiratory reflexes and increase alertness in response to its pungent odor. This product is marketed as an over-the-counter monograph drug, meaning it follows established FDA rules for its category rather than undergoing individual application review.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
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.

🧪 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 70LDW53ROO
    Cotton is a natural fiber derived from cotton plants. It's used as a filler or absorbent material in some medicines to help maintain product consistency and stability.
  • UNII V95R5KMY2B
    Peppermint is a flavoring agent derived from the peppermint plant. It's added to medicines to improve taste and mask bitter or unpleasant flavors, making them easier to take.

2 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesCotton Peppermint Flavour

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.

💲 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
First Aid Only Ammonia Inhalants .045 g/.3mL 00924-5401-01 Acme 10 ampules — — FDA listed —
Ammonia Inhalants .045 g/.3mL 46414-3333-02 James 100 ampules — — FDA listed —
Ammonia Inhalants .05 g/.33mL 67777-0251-01 Dynarex 33 ml — — FDA listed —
Ammonia .15 g/g 68599-7100-01 McKesson 15 g — — Discontinued —
ammonia inhalants .045 g/.3mL 82749-0150-02 Epic 100 ampules — — FDA listed —
Allbizr Iron Shogun Smelling Salts 15 g/100g 85209-0011-01 Hong 65 g — — FDA listed —
Lepnuns SMELLING SALTS 15 g/100g 85248-0021-01 Jiangxi 40 g — — FDA listed —
WXMX Smelling Salts 15 g/100g 85248-0028-01 Jiangxi 50 g — — FDA listed —
Botasun Smelling Salts 15 g/100g 85248-0035-01 Jiangxi 40 g — — FDA listed —
Flobow SMELLING SALTS 15 g/100g 85248-0098-01 Jiangxi 40 g — — FDA listed —
Serynth Smelling Salts 15 g/100g 85248-0105-01 Jiangxi 40 g — — FDA listed —
Sylvirene Smelling Salts 15 g/100g 85248-0140-01 Jiangxi 40 g — — FDA listed —
Reinreude Smelling Salts 15 g/100g 85248-0152-01 Jiangxi 40 g — — FDA listed —
Ottffss Smelling Salts 15 g/100g 85248-0179-01 Jiangxi 40 g — — FDA listed —
Nrmrqz SMELLING SALTS 15 g/100g 85248-0182-01 Jiangxi 40 g — — FDA listed —
LukGain SMELLING SALTS 15 g/100g 85248-0186-01 Jiangxi 40 g — — FDA listed —
Rhinoost SMELLING SALTS 15 g/100g 85248-0193-01 Jiangxi 50 g — — FDA listed —
Unikinesys SMELLING SALTS 15 g/100g 85248-0197-01 Jiangxi 50 g — — FDA listed —
Hoxlbin SMELLING SALTS 15 g/100g 85248-0198-01 Jiangxi 50 g — — FDA listed —
smelling salts SMELLING SALTS 15 g/100g 85248-0225-01 Jiangxi 40 g — — FDA listed —
TideFresh SMELLING SALTS 15 g/100g 85248-0231-01 Jiangxi 40 g — — FDA listed —
Thitfam Smelling Salts 15 g/100g 85248-0234-01 Jiangxi 30 g — — FDA listed —
ANTYZE Smelling Salts 15 g/100g 85590-0001-01 Shenzhen 30 g — — FDA listed —
Gluvelop SMELLING SALTS 15 g/100g 85590-0002-01 Shenzhen 30 g — — FDA listed —
UpSniff Smelling Salts 15 g/100g 85590-0003-01 Shenzhen 30 g — — FDA listed —
TEHCIN smelling salts 15 g/100g 85593-0117-01 Guangzhou 60 g — — Discontinued —
Summit Smelling Salts 15 g/100g 85764-0001-01 Washburn 40 g — — FDA listed —
smelling salts 15 g/100g 85765-0001-01 Shenzhen 30 g — — Discontinued —
smelling salts 15 g/100g 85765-0002-01 Shenzhen 1 bottle — — Discontinued —
smelling salts .15 g/g 85765-0003-01 Shenzhen 50 g — — Discontinued —
ammonia inhalants 15 g/100mL 85813-0003-01 Direct 50 ampules — — FDA listed —
Smelling Salts 15 g/100g 85821-0001-01 Shenzhen 30 g — — FDA listed —
Smelling Salts .15 g/g 85839-0005-01 Shenzhen 30 g — — FDA listed —
Allbiz Sealed Oni Smelling Salts .15 g/g 85920-0001-01 Foshan 50 g — — Discontinued —
Allbiz Sealed Oni Smelling Salts 15 g/100g 85920-0002-01 Foshan 40 g — — Discontinued —
Allbiz Mint Oni Smelling Salts 15 g/100g 85920-0003-01 Foshan 65 g — — Discontinued —
Smelling Salt 4.5 g/30gthis 85999-0001-01 Nanning 30 g — — Discontinued —
Smelling Salt 15 g/100g 87055-0001-01 Guangzhou 30 g — — Discontinued —
Smelling Salt 4.5 g/30g 87175-0001-01 Guangzhou 30 g — — FDA listed —
Palinoia Ammonia Inhalant 15 g/100g 87176-0002-02 Centeroblivion 1 bottle — — Discontinued —
Smelling Salt 4.5 g/30g 87248-0001-01 Shenzhen 30 g — — FDA listed —
Snap Labs Ammonia Inhalants 150 mg/mL 87270-0001-01 Brined 1 jar — — FDA listed —
Snap Labs 20-Count Ammonia Inhalants 150 mg/mL 87270-0002-01 Brined 1 jar — — FDA listed —
Snap Labs Ammonia Inhalants 150 mg/mL 87270-0003-02 Brined 1 jar — — FDA listed —
Snap Labs Ammonia Inhalants 150 mg/mL 87270-0004-01 Brined 1 jar — — FDA listed —
Smelling Salts 15 g/100g 87585-0001-01 Guangzhou 40 g — — FDA listed —
Smelling Salts 15 g/100g 87592-0001-01 Shenzhen 30 g — — FDA listed —
Smelling Salts 15 g/100g 87711-0001-01 Hodayfa 30 g — — 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

🏛️
2025
On the market since
Aug 2025
📍
2026
Currently FDA-listed
1 year 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.

🔬 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 Smelling Salt (this brand).

Top reported reactions

Cerebrovascular Accident1
Intracranial Aneurysm1

Age at onset

Elderly1

Reporter sex

1 reports
Female · 100%

Serious outcomes

Hospitalization1
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
85999-0001-01 You're viewing this 30 g in 1 BOTTLE (85999-001-01) 2025-08-07 Inactivated by FDA

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product No longer marketed (per FDA listing data)
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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 FDA registers it as 85999-001-01, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 85999-0001-01, written without dashes as 85999000101. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 85999-0001-01, the first segment (85999) is the labeler code FDA assigned to Nanning Xingshuang Network Technology Studio (A Sole Proprietorship); the middle segment (0001) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) identifies this exact package size and type. Together they name one specific package of one specific product.
Who lists this product with the FDA?
Nanning Xingshuang Network Technology Studio (A Sole Proprietorship) 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.

📄 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
🎯 Indications and Usage 5 words ▾

Uses:To prevent or treat fainting

⏱️ Dosage and Administration 20 words ▾

Directions:1.Hold bottle 10-15 cm from nostrils and inhale slowly 1-2 times2. Seal tightly after each use to prevent prolonged exposure.

⚠️ Warnings 32 words ▾

Avoid contact with skin or eyes. Rinse immediately with water for 15 minutes ifexposed. Flammable. Keep away from heat, fames, or sparks. For emergency use only. Not a substitute for professional medica!

🧪 Active Ingredient 3 words ▾

Ammonium Carbonate 15%

🧪 Inactive Ingredients 3 words ▾

Cotton Peppermint Flavour

🎯 Purpose 1 words ▾

Inhalant

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 85998-0001-01 · Guangzhou 86014-0200-01 · McKinley →
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.