natural liquidmineralspray

Generic: sodium chloride

Labeler: k-la-ko co.,ltd
NDC Directory HUMAN OTC DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name natural liquidmineralspray
Generic Name sodium chloride
Labeler k-la-ko co.,ltd
Dosage Form LIQUID
Routes
TOPICAL
Active Ingredients

sodium chloride 100 g/100mL

Manufacturer
K-LA-KO Co.,LTD

Identifiers & Regulatory

Product NDC 87034-0002
Product ID 87034-0002_3d26d608-27b3-86f3-e063-6394a90abd83
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2025-06-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 870340002
Hyphenated Format 87034-0002

Supplemental Identifiers

UNII
451W47IQ8X

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 natural liquidmineralspray (source: ndc)
Generic Name sodium chloride (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 100 g/100mL
source: ndc
Packaging
  • 100 mL in 1 BOTTLE, SPRAY (87034-0002-1)
source: ndc

Packages (1)

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

Ingredients (1)

sodium chloride (100 g/100mL)

Linked Drug Pages (1)

NATURAL LIQUIDMINERALSPRAY ndc-match (0.9)

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"}