Rugby Anti-Itch

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: Rugby Anti-Itch
Generic name: CAMPHOR, MENTHOL
Manufacturer: RUGBY LABORATORIES
Product type: HUMAN OTC DRUG
SPL set ID: 99d8ad9e-46ec-15fc-e053-2995a90a0d17
SPL ID: 29a27bb2-2ee1-6e6d-e063-6394a90a4fb2
Version: 7
Effective date: 2024-12-19
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:24:39

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Rugby Anti-Itch	openfda.brand_name
generic name		CAMPHOR, MENTHOL	openfda.generic_name
manufacturer name		RUGBY LABORATORIES	openfda.manufacturer_name
ndc	package	0536-1268-12	openfda.package_ndc
ndc	product	0536-1268	openfda.product_ndc
ndc11	package	00536126812	derived:openfda.package_ndc
rxcui		200176	openfda.rxcui
spl id		29a27bb2-2ee1-6e6d-e063-6394a90a4fb2	id
spl set id		99d8ad9e-46ec-15fc-e053-2995a90a0d17	set_id
unii		L7T10EIP3A	openfda.unii
unii		5TJD82A1ET	openfda.unii

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

Warning For external use only when using this product do not get into eyes Stop Use and ask doctor if condition worsens symptoms last 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 Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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