Package 87034-0002-1

Brand: natural liquidmineralspray

Generic: sodium chloride
NDC Package

Package Facts

Identity

Package NDC 87034-0002-1
Digits Only 8703400021
Product NDC 87034-0002
Description

100 mL in 1 BOTTLE, SPRAY (87034-0002-1)

Marketing

Marketing Status
Marketed Since 2025-06-01
Brand natural liquidmineralspray
Generic sodium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3d26d608-27b3-86f3-e063-6394a90abd83", "openfda": {"unii": ["451W47IQ8X"], "spl_set_id": ["3d26d608-27b1-86f3-e063-6394a90abd83"], "manufacturer_name": ["K-LA-KO Co.,LTD"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE, SPRAY (87034-0002-1)", "package_ndc": "87034-0002-1", "marketing_start_date": "20250601"}], "brand_name": "NATURAL LIQUIDMINERALSPRAY", "product_id": "87034-0002_3d26d608-27b3-86f3-e063-6394a90abd83", "dosage_form": "LIQUID", "product_ndc": "87034-0002", "generic_name": "SODIUM CHLORIDE", "labeler_name": "K-LA-KO Co.,LTD", "product_type": "HUMAN OTC DRUG", "brand_name_base": "NATURAL LIQUIDMINERALSPRAY", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "100 g/100mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20250601", "listing_expiration_date": "20261231"}