numbing cream
Generic: pramoxine hydrochloride 1%
Labeler: bloomwell gardens llcDrug Facts
Product Profile
Brand Name
numbing cream
Generic Name
pramoxine hydrochloride 1%
Labeler
bloomwell gardens llc
Dosage Form
CREAM
Routes
Active Ingredients
pramoxine hydrochloride 1 g/100g
Manufacturer
Identifiers & Regulatory
Product NDC
85284-008
Product ID
85284-008_3c404ff7-8b89-9f6b-e063-6294a90a2d91
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2025-08-13
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
85284008
Hyphenated Format
85284-008
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
numbing cream (source: ndc)
Generic Name
pramoxine hydrochloride 1% (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/100g
Packaging
- 50 g in 1 BOTTLE (85284-008-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3c404ff7-8b89-9f6b-e063-6294a90a2d91", "openfda": {"unii": ["88AYB867L5"], "rxcui": ["1052684"], "spl_set_id": ["3c404ff7-8b88-9f6b-e063-6294a90a2d91"], "manufacturer_name": ["BLOOMWELL GARDENS LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 g in 1 BOTTLE (85284-008-01)", "package_ndc": "85284-008-01", "marketing_start_date": "20250813"}], "brand_name": "Numbing cream", "product_id": "85284-008_3c404ff7-8b89-9f6b-e063-6294a90a2d91", "dosage_form": "CREAM", "product_ndc": "85284-008", "generic_name": "Pramoxine Hydrochloride 1%", "labeler_name": "BLOOMWELL GARDENS LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Numbing cream", "active_ingredients": [{"name": "PRAMOXINE HYDROCHLORIDE", "strength": "1 g/100g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250813", "listing_expiration_date": "20261231"}