ammonia inhalants

Generic: ammonia inhalants

Labeler: dynarex corporation
NDC Directory HUMAN OTC DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name ammonia inhalants
Generic Name ammonia inhalants
Labeler dynarex corporation
Dosage Form INHALANT
Routes
RESPIRATORY (INHALATION)
Active Ingredients

ammonia .05 g/.33mL

Manufacturer
Dynarex Corporation

Identifiers & Regulatory

Product NDC 67777-251
Product ID 67777-251_3c176ea9-62a1-b86f-e063-6294a90ab8f7
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 1976-02-14

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67777251
Hyphenated Format 67777-251

Supplemental Identifiers

RxCUI
1299889
UPC
0616784140124
UNII
5138Q19F1X

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name ammonia inhalants (source: ndc)
Generic Name ammonia inhalants (source: ndc)
Routes
RESPIRATORY (INHALATION)
source: ndc

Resolved Composition

Strengths
  • .05 g/.33mL
source: ndc
Packaging
  • 50 BOX in 1 CASE (67777-251-02) / 10 AMPULE in 1 BOX (67777-251-01) / .33 mL in 1 AMPULE
source: ndc

Packages (1)

Ingredients (1)

ammonia (.05 g/.33mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "3c176ea9-62a1-b86f-e063-6294a90ab8f7", "openfda": {"upc": ["0616784140124"], "unii": ["5138Q19F1X"], "rxcui": ["1299889"], "spl_set_id": ["91e27f1c-0f74-413e-97ff-2fc013f22ca8"], "manufacturer_name": ["Dynarex Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 BOX in 1 CASE (67777-251-02)  / 10 AMPULE in 1 BOX (67777-251-01)  / .33 mL in 1 AMPULE", "package_ndc": "67777-251-02", "marketing_start_date": "19760214"}], "brand_name": "Ammonia Inhalants", "product_id": "67777-251_3c176ea9-62a1-b86f-e063-6294a90ab8f7", "dosage_form": "INHALANT", "product_ndc": "67777-251", "generic_name": "Ammonia Inhalants", "labeler_name": "Dynarex Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ammonia Inhalants", "active_ingredients": [{"name": "AMMONIA", "strength": ".05 g/.33mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "19760214", "listing_expiration_date": "20261231"}