Sunset Novelties Herquake

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: Sunset Novelties Herquake
Generic name: NUMBING LUBRICANT
Manufacturer: SUNSET INTIMATES GROUP INC
Product type: HUMAN OTC DRUG
SPL set ID: 2ceeca3e-9197-9166-e063-6394a90ae908
SPL ID: 2ceeca3e-9198-9166-e063-6394a90ae908
Version: 1
Effective date: 2025-01-30
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 05:53:57

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Sunset Novelties Herquake	openfda.brand_name
generic name		NUMBING LUBRICANT	openfda.generic_name
manufacturer name		SUNSET INTIMATES GROUP INC	openfda.manufacturer_name
ndc	package	85243-111-11	openfda.package_ndc
ndc	product	85243-111	openfda.product_ndc
ndc11	package	85243011111	derived:openfda.package_ndc
spl id		2ceeca3e-9198-9166-e063-6394a90ae908	id
spl set id		2ceeca3e-9197-9166-e063-6394a90ae908	set_id
unii		V13007Z41A	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

Warnings For external use only. Do not use this product with a mechanical device. Certain persons can develop allergic reactions to ingredients in this product. If the symptom being treated does not subside or if redness, irritation, swelling, pain or other symptoms develop or increase, discontinue use and consult a doctor. Do not exceed the daily recommended dosage. In case of any bleeding, discontinue use and consult a doctor. Keep this and all drugs out of reach of children. In case of accidential overdose, seek medical help or call a Poison Control Center right away. As with any drug, consult a health care professional if you are pregnant or nursing. Ask a health care professional before using this product.

Reported adverse events (FAERS/openFDA)#

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