Home FDA labels 30502321-9e0b-f1e0-e063-6394a90a4ed2 Dr Talbots Cooling Perineal Pad 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 Dr Talbots Cooling Perineal Pad
Generic name WATER, ALOE BARBADENSIS LEAF JUICE, BIOFLAVONOIDS, CALENDULA OFFICINALIS FLOWER EXTRACT, CHAMOMILLA RECUTITA FLOWER EXTRACT, CITRIC ACID, DECYL GLUCOSIDE, GLYCERIN, LACTIC ACID, LEVULINIC ACID, MENTHA PIPERITA (PEPPERMINT) OIL, SODIUM COCOAMPHOACETATE, POTASSIUM SORBATE
Manufacturer Talbot's Pharmaceuticals family Products, LLC.
Product type HUMAN OTC DRUG
SPL set ID 242277e2-ff26-ad4e-e063-6394a90ab317
SPL ID 30502321-9e0b-f1e0-e063-6394a90a4ed2
Version 2
Effective date 2025-03-14
Source export date 2026-10-12
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/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:18:46 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 · 11 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field application number M016 openfda.application_number brand name Dr Talbots Cooling Perineal Pad openfda.brand_name generic name WATER, ALOE BARBADENSIS LEAF JUICE, BIOFLAVONOIDS, CALENDULA OFFICINALIS FLOWER EXTRACT, CHAMOMILLA RECUTITA FLOWER EXTRACT, CITRIC ACID, DECYL GLUCOSIDE, GLYCERIN, LACTIC ACID, LEVULINIC ACID, MENTHA PIPERITA (PEPPERMINT) OIL, SODIUM COCOAMPHOACETATE, POTASSIUM SORBATE openfda.generic_name manufacturer name Talbot's Pharmaceuticals family Products, LLC. openfda.manufacturer_name ndc package 70797-104-01 openfda.package_ndc ndc product 70797-104 openfda.product_ndc ndc11 package 70797010401 derived:openfda.package_ndc rxcui 844379 openfda.rxcui spl id 30502321-9e0b-f1e0-e063-6394a90a4ed2 id spl set id 242277e2-ff26-ad4e-e063-6394a90ab317 set_id unii 101I4J0U34 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 For external use only: Avoid contact with eye. If contact occurs, rinse thoroughly with water. Do not exceed the recommended daily dosage unless directed by doctor. Do not put this product in the rectum by using fingers or any mechanical device or applicator. Warning Section
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.