PRIME PULSE SMELLING SALTS

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerDirect Outlet Supplier LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8581300201
47 g in 1 BOTTLE (85813-002-01)

Annotations

UNII (FDA Substance ID)

NJ5VT0FKLJ

AMMONIUM CARBONATE

RxCUI 1310190

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "NJ5VT0FKLJ",
    "rxcui": "1310190",
    "inchikey": null,
    "display_name": "AMMONIUM CARBONATE",
    "substance_type": "mixture",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "RESPIRATORY (INHALATION)",
  "spl_meta": {
    "55e95657-9415-4d9c-ac9b-d021aa14e64d": {
      "match": "brand_token",
      "title": "PRIME TOOTH CARE COCONUT WHIP (SODIUM FLUORIDE) OINTMENT [PRIME TOOTH CARE LLC]",
      "spl_version": "2",
      "published_date": "2026-01-30"
    }
  },
  "productid": "85813-002_2e8917d0-05ca-4a52-b635-3a6ed90bdb02",
  "productndc": "85813-002",
  "dosage_form": "GRANULE",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AMMONIUM CARBONATE; SODIUM CARBONATE",
  "proprietary_name": "PRIME PULSE SMELLING SALTS",
  "active_ingred_unit": "g/100g; g/100g",
  "application_number": "M011",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Ammonium Carbonate and Sodium Carbonate",
  "start_marketing_date": "20251126",
  "active_numerator_strength": "15; 10"
}

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