instant

Generic: instant

Labeler: ultra-chem, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name instant
Generic Name instant
Labeler ultra-chem, inc.
Dosage Form LIQUID
Routes
TOPICAL
Active Ingredients

alcohol 67 mL/100mL

Manufacturer
Ultra-Chem, Inc.

Identifiers & Regulatory

Product NDC 66077-693
Product ID 66077-693_0c42240b-580d-eb4f-e063-6394a90a24ee
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2026-12-31
Marketing Start 2010-10-18

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 66077693
Hyphenated Format 66077-693

Supplemental Identifiers

UNII
3K9958V90M

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 instant (source: ndc)
Generic Name instant (source: ndc)
Application Number 505G(a)(3) (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 67 mL/100mL
source: ndc
Packaging
  • 118 mL in 1 BOTTLE, PLASTIC (66077-693-01)
source: ndc

Packages (1)

66077-693-01 118 mL in 1 BOTTLE, PLASTIC (66077-693-01)

Ingredients (1)

alcohol (67 mL/100mL)

Linked Drug Pages (1)

INSTANT ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "0c42240b-580d-eb4f-e063-6394a90a24ee", "openfda": {"unii": ["3K9958V90M"], "spl_set_id": ["0c425c6e-6c05-1748-e063-6394a90a9b5e"], "manufacturer_name": ["Ultra-Chem, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE, PLASTIC (66077-693-01)", "package_ndc": "66077-693-01", "marketing_start_date": "20101018"}], "brand_name": "INSTANT", "product_id": "66077-693_0c42240b-580d-eb4f-e063-6394a90a24ee", "dosage_form": "LIQUID", "product_ndc": "66077-693", "generic_name": "INSTANT", "labeler_name": "Ultra-Chem, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "INSTANT", "active_ingredients": [{"name": "ALCOHOL", "strength": "67 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20101018", "listing_expiration_date": "20261231"}