ALLBIZ SEALED ONI SMELLING SALTS

Manufacturer
Foshan Nanhai District Didi Didi E Commerce Co., Ltd.
Effective date
2025-07-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:08:15

Label at a glance#

ProductALLBIZ SEALED ONI SMELLING SALTS
Active ingredientAMMONIA
Label structure13 sections

Dosage and administration

Hold bottle 10-15 cm (4-6 inches) from nostrils. Inhale gently. Do not place directly inside the nostrils. Do not inhale for more than 2 seconds per use. Do not use more than once every 60 minutes. Do not use more than 10 times per day. Use only as needed. If symptoms persist, consult a healthcare professional.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ammonia 15%

OTC - PURPOSE SECTION

Inhalant

Use

INDICATIONS & USAGE SECTION

For the temporary stimulation of the senses to restore alertness.

Warnings

WARNINGS SECTION

For inhalation use only.
Do not ingest or apply to skin.
Avoid direct contact with eyes. If contact occurs, rinse thoroughly with water for 15 minutes.
Use only as directed. Misuse may be harmful.
Use in a well-ventilated area. Do not use in enclosed spaces.
Prolonged exposure may cause irritation. Discontinue use if discomfort occurs.
Possible side effects include nasal irritation, coughing, or shortness of breath. If symptoms persist, discontinue use and consult a doctor.

Do not use

OTC - DO NOT USE SECTION

If you have respiratory conditions such as asthma or emphysema.
If you have heart disease or high blood pressure.
If you are allergic to ammonia or strong odors.

When Using

OTC - WHEN USING SECTION

Avoid contact with eyes, ears, and mouth.
If product gets into eyes, rinse thoroughly with water for 15 minutes.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

ask a doctor

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately at 1-800-222-1222.

Directions

DOSAGE & ADMINISTRATION SECTION

Hold bottle 10-15 cm (4-6 inches) from nostrils.
Inhale gently. Do not place directly inside the nostrils.
Do not inhale for more than 2 seconds per use.
Do not use more than once every 60 minutes.
Do not use more than 10 times per day.
Use only as needed. If symptoms persist, consult a healthcare professional.

Other information

OTHER SAFETY INFORMATION

Store in a cool, dry place at 15-25°C (59-77°F).
Avoid freezing, excessive heat above 40°C (104°F), and direct sunlight.
Do not use if safety seal under cap is broken .

INACTIVE INGREDIENT SECTION

Alcohol, Cotton, Peppermint Oil.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labelinglabeling

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1299889ammonia 15 % Nasal InhalantPSN1
1299889ammonia 150 MG/ML Nasal InhalantSCD1
1299889ammonia 0.045 GM per 0.3 ML Nasal InhalantSY1
1299889ammonia 0.3 ML Nasal InhalantSY1
1299889ammonia 15 % Nasal InhalantSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85920-002-01ALLBIZ SEALED ONI SMELLING SALTS40 g in 1 BOTTLEINHALANT401

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85920-00285920-002-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
AMMONIA5138Q19F1XACTIB
PEPPERMINT OILAV092KU4JHIACT
COTTON70LDW53ROOIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
3a87c99b-5517-fcc4-e063-6294a90a7b923a87c99b-5516-fcc4-e063-6294a90a7b922025-07-22WarningsExact identifier
spl id: 3a87c99b-5517-fcc4-e063-6294a90a7b92
spl set id: 3a87c99b-5516-fcc4-e063-6294a90a7b92

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.