licefreee afterlice
Generic: pramoxine hci
Labeler: tec laboratories inc.Drug Facts
Product Profile
Brand Name
licefreee afterlice
Generic Name
pramoxine hci
Labeler
tec laboratories inc.
Dosage Form
SPRAY
Routes
Active Ingredients
pramoxine hydrochloride 10 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
51879-260
Product ID
51879-260_262f50ab-fd53-7474-e063-6394a90a4f40
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2023-10-16
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51879260
Hyphenated Format
51879-260
Supplemental Identifiers
RxCUI
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
licefreee afterlice (source: ndc)
Generic Name
pramoxine hci (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/g
Packaging
- 177.4 g in 1 BOTTLE, PLASTIC (51879-260-06)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "262f50ab-fd53-7474-e063-6394a90a4f40", "openfda": {"unii": ["88AYB867L5"], "rxcui": ["1294036"], "spl_set_id": ["06c4cc42-a215-3949-e063-6394a90a665e"], "manufacturer_name": ["Tec Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "177.4 g in 1 BOTTLE, PLASTIC (51879-260-06)", "package_ndc": "51879-260-06", "marketing_start_date": "20231016"}], "brand_name": "Licefreee AfterLice", "product_id": "51879-260_262f50ab-fd53-7474-e063-6394a90a4f40", "dosage_form": "SPRAY", "product_ndc": "51879-260", "generic_name": "Pramoxine HCI", "labeler_name": "Tec Laboratories Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Licefreee AfterLice", "active_ingredients": [{"name": "PRAMOXINE HYDROCHLORIDE", "strength": "10 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20231016", "listing_expiration_date": "20261231"}