After Bite Outdoor

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
After Bite Outdoor
Generic name
DIPHENHYDRAMINE HCL
Manufacturer
Tender Corporation d/b/a Adventure Ready Brands
Product type
HUMAN OTC DRUG
SPL set ID
22b891a9-6386-dee1-e063-6394a90a5c2f
SPL ID
4395c743-e625-1ba6-e063-6294a90a33db
Version
2
Effective date
2025-11-14
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:54:42
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only Do not use on large areas of the body, with any other product containing diphenhydramine, even one taken by mouth. Ask a doctor before use On chicken pox, on measles when using this product Avoid contact with eyes. Stop use and ask a doctor if Condition worsens, if symptoms persist more than 7 days or clear up and occur again within a few days Keep out of reach of children If swallowed, get medical help or contact a Posion Control Center right away.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.