PRIME PULSE SMELLING SALTS

Product NDC
85813-002
11-digit product format
858130002
Labeler code
85813
Product ID
85813-002_2e8917d0-05ca-4a52-b635-3a6ed90bdb02
Type
HUMAN OTC DRUG
Nonproprietary name
Ammonium Carbonate and Sodium Carbonate
Dosage form
GRANULE
Route
RESPIRATORY (INHALATION)
Labeler
Direct Outlet Supplier LLC
Application
M011
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-11-26
Substance
AMMONIUM CARBONATE; SODIUM CARBONATE
Active strength
15; 10 g/100g; g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
PRIME PULSE SMELLING SALTS
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AMMONIUM CARBONATE15 g/100g
SODIUM CARBONATE10 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiNJ5VT0FKLJ, 45P3261C7T
Rxcui2722955

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85813-002-01PRIME PULSE SMELLING SALTS47 g in 1 BOTTLEGRANULE471

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2722955ammonium carbonate 15 % / sodium carbonate 10 % Nasal InhalantPSNbfcb059b-fbb6-44f0-a8ce-fa967a52cf991
2722955ammonium carbonate 150 MG/ML / sodium carbonate 100 MG/ML Nasal InhalantSCDbfcb059b-fbb6-44f0-a8ce-fa967a52cf991
2722955ammonium carbonate 15 % / sodium carbonate 10 % Nasal InhalantSYbfcb059b-fbb6-44f0-a8ce-fa967a52cf991

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85813-002-018581300020147 g in 1 BOTTLE (85813-002-01) 47 g2025-11-26NoNoCurrent