GLUVELOP SMELLING SALTS- smelling salts inhalant

Gluvelop SMELLING SALTS by

Drug Labeling and Warnings

Gluvelop SMELLING SALTS by is a Otc medication manufactured, distributed, or labeled by Shenzhen Nanjun Technology Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ammonia 15%

Purpose

Inhalants

Use

To prevent or treat fainang.

Warnings

For external use only.

Do not use

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

When Using

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

Stop Use

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

Ask Doctor

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

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

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

Other information

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

Alcohol, Cotton,Lemon flavor

Questions

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GLUVELOP SMELLING SALTS 
smelling salts inhalant

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85590-002
Route of Administration	RESPIRATORY (INHALATION)

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X)	AMMONIA	15 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
LIMONENE, (+/-)- (UNII: 9MC3I34447)
ALCOHOL (UNII: 3K9958V90M)
COTTON (UNII: 70LDW53ROO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85590-002-01	30 g in 1 BOTTLE; Type 0: Not a Combination Product	07/10/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M011	07/10/2025

Labeler - Shenzhen Nanjun Technology Co., Ltd (452881391)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Nanjun Technology Co., Ltd		452881391	manufacture(85590-002)