salicylic acid
Generic: wart remover liquid
Labeler: harris teeter, llcDrug Facts
Product Profile
Brand Name
salicylic acid
Generic Name
wart remover liquid
Labeler
harris teeter, llc
Dosage Form
LIQUID
Routes
Active Ingredients
salicylic acid .17 mg/9mL
Manufacturer
Identifiers & Regulatory
Product NDC
69256-035
Product ID
69256-035_40976655-12cc-fd19-e063-6394a90ad3b0
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M028
Listing Expiration
2026-12-31
Marketing Start
2017-12-21
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69256035
Hyphenated Format
69256-035
Supplemental Identifiers
UNII
Packaging Origin
Original Packager
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
salicylic acid (source: ndc)
Generic Name
wart remover liquid (source: ndc)
Application Number
M028 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .17 mg/9mL
Packaging
- 9 mL in 1 BOTTLE, WITH APPLICATOR (69256-035-09)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "40976655-12cc-fd19-e063-6394a90ad3b0", "openfda": {"unii": ["O414PZ4LPZ"], "spl_set_id": ["d53756d4-6739-48da-b367-84531f989170"], "manufacturer_name": ["Harris Teeter, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 mL in 1 BOTTLE, WITH APPLICATOR (69256-035-09)", "package_ndc": "69256-035-09", "marketing_start_date": "20171221"}], "brand_name": "Salicylic Acid", "product_id": "69256-035_40976655-12cc-fd19-e063-6394a90ad3b0", "dosage_form": "LIQUID", "product_ndc": "69256-035", "generic_name": "Wart Remover Liquid", "labeler_name": "Harris Teeter, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Salicylic Acid", "active_ingredients": [{"name": "SALICYLIC ACID", "strength": ".17 mg/9mL"}], "application_number": "M028", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20171221", "listing_expiration_date": "20261231"}