baby mucus plus cold relief daytime and nighttime

Generic: calcium sulfide,phosphorus,sulfur,rumex crispus root,sodium chloride,arabica coffee bean,anemone pulsatilla,silicon dioxide, goldenseal,onion,bryonia alba root,euphrasia stricta and matricaria chamomilla

Labeler: hyland's inc.
NDC Directory HUMAN OTC DRUG UNAPPROVED HOMEOPATHIC Inactive Finished

Drug Facts

Product Profile

Brand Name baby mucus plus cold relief daytime and nighttime
Generic Name calcium sulfide,phosphorus,sulfur,rumex crispus root,sodium chloride,arabica coffee bean,anemone pulsatilla,silicon dioxide, goldenseal,onion,bryonia alba root,euphrasia stricta and matricaria chamomilla
Labeler hyland's inc.
Dosage Form KIT
Manufacturer
Hyland's Inc.

Identifiers & Regulatory

Product NDC 54973-3374
Product ID 54973-3374_0397de56-d497-5ac4-e063-6294a90accb2
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2026-12-31
Marketing Start 2018-11-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 549733374
Hyphenated Format 54973-3374

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 baby mucus plus cold relief daytime and nighttime (source: ndc)
Generic Name calcium sulfide,phosphorus,sulfur,rumex crispus root,sodium chloride,arabica coffee bean,anemone pulsatilla,silicon dioxide, goldenseal,onion,bryonia alba root,euphrasia stricta and matricaria chamomilla (source: ndc)

Resolved Composition

Packaging
  • 1 KIT in 1 CARTON (54973-3374-1) * 118 mL in 1 BOTTLE, PLASTIC (54973-3284-1) * 118 mL in 1 BOTTLE (54973-3371-2)
source: ndc

Packages (1)

54973-3374-1 1 KIT in 1 CARTON (54973-3374-1) * 118 mL in 1 BOTTLE, PLASTIC (54973-3284-1) * 118 mL in 1 BOTTLE (54973-3371-2)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

BABY MUCUS PLUS COLD RELIEF DAYTIME AND NIGHTTIME ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "0397de56-d497-5ac4-e063-6294a90accb2", "openfda": {"spl_set_id": ["7979fc6f-6d2c-56c9-e053-2991aa0ac1f3"], "manufacturer_name": ["Hyland's Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (54973-3374-1)  *  118 mL in 1 BOTTLE, PLASTIC (54973-3284-1)  *  118 mL in 1 BOTTLE (54973-3371-2)", "package_ndc": "54973-3374-1", "marketing_start_date": "20181101"}], "brand_name": "BABY MUCUS PLUS COLD RELIEF DAYTIME AND NIGHTTIME", "product_id": "54973-3374_0397de56-d497-5ac4-e063-6294a90accb2", "dosage_form": "KIT", "product_ndc": "54973-3374", "generic_name": "calcium sulfide,phosphorus,sulfur,rumex crispus root,sodium chloride,arabica coffee bean,anemone pulsatilla,silicon dioxide, goldenseal,onion,bryonia alba root,euphrasia stricta and matricaria chamomilla", "labeler_name": "Hyland's Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "BABY MUCUS PLUS COLD RELIEF DAYTIME AND NIGHTTIME", "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20181101", "listing_expiration_date": "20261231"}