after bite xtra
Generic: diphenhydramine hcl
Labeler: tender corporation d/b/a adventure ready brandsDrug Facts
Product Profile
Brand Name
after bite xtra
Generic Name
diphenhydramine hcl
Labeler
tender corporation d/b/a adventure ready brands
Dosage Form
GEL
Routes
Active Ingredients
diphenhydramine hydrochloride .4 g/20g
Manufacturer
Identifiers & Regulatory
Product NDC
44224-1276
Product ID
44224-1276_401fae13-e670-1754-e063-6394a90a3afe
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2025-01-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
442241276
Hyphenated Format
44224-1276
Supplemental Identifiers
RxCUI
UPC
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
after bite xtra (source: ndc)
Generic Name
diphenhydramine hcl (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .4 g/20g
Packaging
- 1 TUBE in 1 BOX (44224-1276-1) / 1 g in 1 TUBE (44224-1276-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "401fae13-e670-1754-e063-6394a90a3afe", "openfda": {"upc": ["0044224612700"], "unii": ["TC2D6JAD40"], "rxcui": ["1049880"], "spl_set_id": ["22b8b83e-66d6-0caa-e063-6394a90ad6fd"], "manufacturer_name": ["Tender Corporation d/b/a Adventure Ready Brands"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (44224-1276-1) / 1 g in 1 TUBE (44224-1276-0)", "package_ndc": "44224-1276-1", "marketing_start_date": "20250101"}], "brand_name": "After Bite Xtra", "product_id": "44224-1276_401fae13-e670-1754-e063-6394a90a3afe", "dosage_form": "GEL", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "44224-1276", "generic_name": "Diphenhydramine HCl", "labeler_name": "Tender Corporation d/b/a Adventure Ready Brands", "product_type": "HUMAN OTC DRUG", "brand_name_base": "After Bite Xtra", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": ".4 g/20g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250101", "listing_expiration_date": "20261231"}