ProCure ClamaPlex

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: ProCure ClamaPlex
Generic name: ZINC OXIDE 20.625, MENTHOL 0.44, WHITE PETROLATUM 66.335
Manufacturer: Twin Med LLC
Product type: HUMAN OTC DRUG
SPL set ID: 3d366857-5178-9032-e063-6294a90a40f3
SPL ID: 3d366857-5179-9032-e063-6294a90a40f3
Version: 1
Effective date: 2025-11-01
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:28:01

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 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M015	openfda.application_number
brand name		ProCure ClamaPlex	openfda.brand_name
generic name		ZINC OXIDE 20.625, MENTHOL 0.44, WHITE PETROLATUM 66.335	openfda.generic_name
manufacturer name		Twin Med LLC	openfda.manufacturer_name
ndc	package	55681-044-14	openfda.package_ndc
ndc	package	55681-044-04	openfda.package_ndc
ndc	package	55681-044-05	openfda.package_ndc
ndc	product	55681-044	openfda.product_ndc
ndc11	package	55681004404	derived:openfda.package_ndc
ndc11	package	55681004414	derived:openfda.package_ndc
ndc11	package	55681004405	derived:openfda.package_ndc
spl id		3d366857-5179-9032-e063-6294a90a40f3	id
spl set id		3d366857-5178-9032-e063-6294a90a40f3	set_id
unii		L7T10EIP3A	openfda.unii
unii		SOI2LOH54Z	openfda.unii
unii		B6E5W8RQJ4	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 Warnings For external use only Allergy Alert: 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. When using this product When using this product do not exceed the recommended daily dosage unless directed by a doctor do not put this product into the rectum by using fingers or any mechanical device or applicator Stop use and ask doctor if Stop using and ask a doctor if condition worsens or does not improve in 7 days bleeding occurs, consult a doctor promptly Keep out of reach of children Keep out of reach of Children . In case of accidental ingestion, contact a physician or Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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