dermatouch acnecare cleanser
Generic: salicylic acid
Labeler: spa de soleilDrug Facts
Product Profile
Brand Name
dermatouch acnecare cleanser
Generic Name
salicylic acid
Labeler
spa de soleil
Dosage Form
LIQUID
Routes
Active Ingredients
salicylic acid 1.15 mg/230mL
Manufacturer
Identifiers & Regulatory
Product NDC
68062-9005
Product ID
68062-9005_48e041f0-24c4-54d4-e063-6294a90a1b39
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M006
Listing Expiration
2027-12-31
Marketing Start
2022-07-08
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680629005
Hyphenated Format
68062-9005
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
dermatouch acnecare cleanser (source: ndc)
Generic Name
salicylic acid (source: ndc)
Application Number
M006 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1.15 mg/230mL
Packaging
- 230 mL in 1 BOTTLE (68062-9005-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "48e041f0-24c4-54d4-e063-6294a90a1b39", "openfda": {"unii": ["O414PZ4LPZ"], "spl_set_id": ["e3514af1-f9b9-c251-e053-2a95a90ac80e"], "manufacturer_name": ["Spa de Soleil"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "230 mL in 1 BOTTLE (68062-9005-1)", "package_ndc": "68062-9005-1", "marketing_start_date": "20220708"}], "brand_name": "Dermatouch Acnecare Cleanser", "product_id": "68062-9005_48e041f0-24c4-54d4-e063-6294a90a1b39", "dosage_form": "LIQUID", "product_ndc": "68062-9005", "generic_name": "salicylic acid", "labeler_name": "Spa de Soleil", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dermatouch Acnecare Cleanser", "active_ingredients": [{"name": "SALICYLIC ACID", "strength": "1.15 mg/230mL"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220708", "listing_expiration_date": "20271231"}