Package 0220-0432-41

Brand: aqua marina

Generic: sodium chloride
NDC Package

Package Facts

Identity

Package NDC 0220-0432-41
Digits Only 0220043241
Product NDC 0220-0432
Description

30 [hp_C] in 1 TUBE (0220-0432-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand aqua marina
Generic sodium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "08541f82-a6a3-bffb-e063-6294a90a133f", "openfda": {"unii": ["451W47IQ8X"], "spl_set_id": ["6a212a52-32be-21b8-e053-2991aa0aea2f"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-0432-41)", "package_ndc": "0220-0432-41", "marketing_start_date": "19830303"}], "brand_name": "Aqua marina", "product_id": "0220-0432_08541f82-a6a3-bffb-e063-6294a90a133f", "dosage_form": "PELLET", "product_ndc": "0220-0432", "generic_name": "SODIUM CHLORIDE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aqua marina", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}