PRIME PULSE SMELLING SALTS- ammonium carbonate and sodium carbonate granule

PRIME PULSE SMELLING SALTS by

Drug Labeling and Warnings

PRIME PULSE SMELLING SALTS by is a Otc medication manufactured, distributed, or labeled by Direct Outlet Supplier LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Ammonium Carbonate................15%
Sodium Carbonate......................10%

Purpose 

The purpose of Prime Pulse Smelling Salts is to get a boost of energy when going for your max effort sporting events. Whether you are a powerlifter, footballer, weightlifter or any sport that demands high performance this is the product for you. with Prime Pulse you will get Prime Results.

Usage

With the combination of Ammonium Carbonate + Sodium Carbonate added with some water and well shaken,Prime Pulse Smelling Salts will release ammonia gas that irritates the nasal pathways that provides instant fight or flight that will boosts endurance, focus and strength.

Warning and Precautions

Keep away from fire or flame

keep bottle 6 inches from nose.

Keep away from children.

DO NOT USE

Do not use if allergic to any ingredients or pregnant.

Directions 

Product is already pre-activated. Just shake the bottle and sniff!

Inactive Ingredient

Alcohol

Disclaimer

This drug has not been found to be safe by the FDA and effective and this labeling has not been approved by the FDA. This product is not intended to diagnose, treat or cure any disease

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PRIME PULSE SMELLING SALTS 
ammonium carbonate and sodium carbonate granule

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85813-002
Route of Administration	RESPIRATORY (INHALATION)

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMMONIUM CARBONATE (UNII: NJ5VT0FKLJ) (AMMONIUM CATION - UNII:54S68520I4)	AMMONIUM CATION	15 g  in 100 g
SODIUM CARBONATE (UNII: 45P3261C7T) (CARBONATE ION - UNII:7UJQ5OPE7D)	SODIUM CARBONATE	10 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85813-002-01	47 g in 1 BOTTLE; Type 0: Not a Combination Product	11/26/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M011	11/26/2025

Labeler - Direct Outlet Supplier LLC (133619845)