Gluvelop SMELLING SALTS

Manufacturer: Shenzhen Nanjun Technology Co., Ltd
Effective date: 2025-07-09
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:06:55

Label at a glance#

ProductGluvelop SMELLING SALTS

Active ingredientAMMONIA

Label structure14 sections

Dosage and administration

Hold bottle 10-15 cm from nostrils and inhale slowly 1-2 times.

Storage and handling

Net Weight: 30g/1.06oz Expiry Date: 24 months(refer to batch number on bottle base) Storage: Store in a dark, dry place at 15-25°C.

Contacts and useful links#

PhonePoison Help1-800-222-1222

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ammonia 15%

Purpose

OTC - PURPOSE SECTION

Inhalants

Use

INDICATIONS & USAGE SECTION

To prevent or treat fainang.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

Do not use if you have respiratory conditions such as asthma or emphysema.
Discontinue use and consult a doctor if symptoms persist

When Using

OTC - WHEN USING SECTION

Avoid repeated inhalation. Do not use more than 2 times per application.

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if allergic reaction (rash, swelling) or persistent irritation occurs.

Ask Doctor

OTC - ASK DOCTOR SECTION

Do not use if you have respiratory conditions such as asthma or emphysema.
Discontinue use and consult a doctor if symptoms persist.

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Store in a cool, dry place inaccessible to children. Swallowing may cause poisoning.
If swallowed, seek immediate medical assistance or contact a Poison
Control Center(1-800-222-1222).

Directions

DOSAGE & ADMINISTRATION SECTION

Hold bottle 10-15 cm from nostrils and inhale slowly 1-2 times.

Other information

STORAGE AND HANDLING SECTION

Net Weight: 30g/1.06oz
Expiry Date: 24 months(refer to batch number on bottle base)
Storage: Store in a dark, dry place at 15-25°C.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Alcohol, Cotton,Lemon flavor

Questions

OTC - QUESTIONS SECTION

Ifswallowed,seekimmediatemedicalassistanceorcontactaPoison
ControlCenter(1-800-222-1222)

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1299889	ammonia 15 % Nasal Inhalant	PSN	1
1299889	ammonia 150 MG/ML Nasal Inhalant	SCD	1
1299889	ammonia 0.045 GM per 0.3 ML Nasal Inhalant	SY	1
1299889	ammonia 0.3 ML Nasal Inhalant	SY	1
1299889	ammonia 15 % Nasal Inhalant	SY	1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
85590-002-01	Gluvelop SMELLING SALTS	30 g in 1 BOTTLE	INHALANT	30		1

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Gluvelop SMELLING SALTS
SMELLING SALTS
LIMONENE, (+/-)-
ALCOHOL
AMMONIA
COTTON

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
85590-002	85590-002-01

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
Name	UNII	Kind
LIMONENE, (+/-)-	9MC3I34447	IACT
ALCOHOL	3K9958V90M	IACT
AMMONIA	5138Q19F1X	ACTIB
COTTON	70LDW53ROO	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Gluvelop SMELLING SALTS	SMELLING SALTS	Shenzhen Nanjun Technology Co., Ltd	398c26ec-5eba-1202-e063-6294a90a76c9	2025-07-09	Warnings	Exact identifier ndc (package): 85590-002-01 ndc (product): 85590-002 ndc11 (package): 85590000201 spl id: 398c26ec-5ebb-1202-e063-6294a90a76c9 spl set id: 398c26ec-5eba-1202-e063-6294a90a76c9

Reported adverse events (FAERS/openFDA)#

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