after bite xtra

Generic: diphenhydramine hcl

Labeler: tender corporation d/b/a adventure ready brands
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug 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
TOPICAL
Active Ingredients

diphenhydramine hydrochloride .4 g/20g

Manufacturer
Tender Corporation d/b/a Adventure Ready Brands

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
histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 442241276
Hyphenated Format 44224-1276

Supplemental Identifiers

RxCUI
1049880
UPC
0044224612700
UNII
TC2D6JAD40

Packaging Origin

Original Packager
true

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
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .4 g/20g
source: ndc
Packaging
  • 1 TUBE in 1 BOX (44224-1276-1) / 1 g in 1 TUBE (44224-1276-0)
source: ndc

Packages (1)

Ingredients (1)

diphenhydramine hydrochloride (.4 g/20g)

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"}