dr lift blemish
Generic: salicylic acid
Labeler: spa de soleilDrug Facts
Product Profile
Brand Name
dr lift blemish
Generic Name
salicylic acid
Labeler
spa de soleil
Dosage Form
LOTION
Routes
Active Ingredients
salicylic acid 1 mg/100mL, sulfur 2 mg/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
68062-2265
Product ID
68062-2265_48dfd489-9f9b-ff51-e063-6294a90a25b0
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M006
Listing Expiration
2027-12-31
Marketing Start
2023-06-27
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680622265
Hyphenated Format
68062-2265
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
dr lift blemish (source: ndc)
Generic Name
salicylic acid (source: ndc)
Application Number
M006 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/100mL
- 2 mg/100mL
Packaging
- 100 mL in 1 BOTTLE (68062-2265-1)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "48dfd489-9f9b-ff51-e063-6294a90a25b0", "openfda": {"unii": ["O414PZ4LPZ", "70FD1KFU70"], "spl_set_id": ["ff2974d3-39e0-0fcc-e053-6294a90a0f3e"], "manufacturer_name": ["Spa de Soleil"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (68062-2265-1)", "package_ndc": "68062-2265-1", "marketing_start_date": "20230627"}], "brand_name": "Dr Lift Blemish", "product_id": "68062-2265_48dfd489-9f9b-ff51-e063-6294a90a25b0", "dosage_form": "LOTION", "product_ndc": "68062-2265", "generic_name": "salicylic acid", "labeler_name": "Spa de Soleil", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dr Lift Blemish", "active_ingredients": [{"name": "SALICYLIC ACID", "strength": "1 mg/100mL"}, {"name": "SULFUR", "strength": "2 mg/100mL"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230627", "listing_expiration_date": "20271231"}