acne gel pen
Generic: salicylic acid
Labeler: tiege hanleyDrug Facts
Product Profile
Brand Name
acne gel pen
Generic Name
salicylic acid
Labeler
tiege hanley
Dosage Form
GEL
Routes
Active Ingredients
salicylic acid 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
71714-004
Product ID
71714-004_4176d9b1-ca94-a6c4-e063-6394a90a68fb
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M006
Listing Expiration
2026-12-31
Marketing Start
2025-10-31
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71714004
Hyphenated Format
71714-004
Supplemental Identifiers
RxCUI
UPC
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
acne gel pen (source: ndc)
Generic Name
salicylic acid (source: ndc)
Application Number
M006 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 1.3 mL in 1 TUBE, WITH APPLICATOR (71714-004-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4176d9b1-ca94-a6c4-e063-6394a90a68fb", "openfda": {"upc": ["0850061136503"], "unii": ["O414PZ4LPZ"], "rxcui": ["346298"], "spl_set_id": ["4176d9b1-ca93-a6c4-e063-6394a90a68fb"], "manufacturer_name": ["Tiege Hanley"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1.3 mL in 1 TUBE, WITH APPLICATOR (71714-004-01)", "package_ndc": "71714-004-01", "marketing_start_date": "20251031"}], "brand_name": "Acne Gel Pen", "product_id": "71714-004_4176d9b1-ca94-a6c4-e063-6394a90a68fb", "dosage_form": "GEL", "product_ndc": "71714-004", "generic_name": "Salicylic Acid", "labeler_name": "Tiege Hanley", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acne Gel Pen", "active_ingredients": [{"name": "SALICYLIC ACID", "strength": "20 mg/mL"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251031", "listing_expiration_date": "20261231"}