acne face and body
Generic: benzoyl peroxide
Labeler: face reality, inc.Drug Facts
Product Profile
Brand Name
acne face and body
Generic Name
benzoyl peroxide
Labeler
face reality, inc.
Dosage Form
SHAMPOO, SUSPENSION
Routes
Active Ingredients
benzoyl peroxide 25 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70707-101
Product ID
70707-101_0c864f2d-7b4f-370e-e063-6394a90ae1a4
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M006
Listing Expiration
2026-12-31
Marketing Start
2011-09-15
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
70707101
Hyphenated Format
70707-101
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
acne face and body (source: ndc)
Generic Name
benzoyl peroxide (source: ndc)
Application Number
M006 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/mL
Packaging
- 180 mL in 1 BOTTLE (70707-101-06)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "0c864f2d-7b4f-370e-e063-6394a90ae1a4", "openfda": {"unii": ["W9WZN9A0GM"], "spl_set_id": ["454983d2-4b00-6268-e054-00144ff8d46c"], "manufacturer_name": ["Face Reality, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 mL in 1 BOTTLE (70707-101-06)", "package_ndc": "70707-101-06", "marketing_start_date": "20161230"}], "brand_name": "Acne Face and Body", "product_id": "70707-101_0c864f2d-7b4f-370e-e063-6394a90ae1a4", "dosage_form": "SHAMPOO, SUSPENSION", "product_ndc": "70707-101", "generic_name": "BENZOYL PEROXIDE", "labeler_name": "Face Reality, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acne Face and Body", "active_ingredients": [{"name": "BENZOYL PEROXIDE", "strength": "25 mg/mL"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110915", "listing_expiration_date": "20261231"}