Dermaplex PrePost JPN

Manufacturer
BouMatic, LLC
Effective date
2021-05-26
Label type
OTC ANIMAL DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:40:59

Label at a glance#

ProductDermaplex PrePost JPN
Active ingredientLACTIC ACID
Label structure4 sections

Dosage and administration

NOT FOR HUMAN USE FOR EXTERNAL USE ONLY USE AT FULL STRENGTH FIRST AID: If in eyes: Hold eye open and rinse slowly and gently with water for 15-20 minutes. Remove contact lenses, if present after the first 5 minutes, then continue rinsing. Contact a physician immediately. If swallowed: Have person sip a glass of water if able to swallow. Do not give anything to an unconscious person. Do not induce vomiting. Contac...

Storage and handling

Store in a closed container away from sources of heat. If product becomes frozen, thaw and mix well before use.

Label contents#

Full prescribing information#

USE DIRECTIONS

GENERAL PRECAUTIONS SECTION

NOT FOR HUMAN USE
FOR EXTERNAL USE ONLY
USE AT FULL STRENGTH

FIRST AID:
If in eyes: Hold eye open and rinse slowly and gently with water for 15-20 minutes. Remove contact lenses,
if present after the first 5 minutes, then continue rinsing. Contact a physician immediately. If swallowed:
Have person sip a glass of water if able to swallow. Do not give anything to an unconscious person. Do not
induce vomiting. Contact a physician immediately. If breathing difficulty occurs: Move person to fresh air.
Contact a physician immediately. If on skin: Take off contaminated clothing. Rinse skin with soap and water.
If irritation develops and persists, contact a physician.
Have the product container or label with you when going for treatment, calling a physician, the emergency
number listed on this label or MSDS, or a poison control center.

Storage:

STORAGE AND HANDLING SECTION

Store in a closed container away from sources of heat. If product becomes frozen, thaw and mix
well before use.

PRE-DIPPING AND POST-DIPPING INSTRUCTIONS

INSTRUCTIONS FOR USE SECTION

PRE-DIPPING: BEFORE MILKING, DIP OR SPRAY ENTIRE TEAT WITH THIS PRODUCT. WIPE TEATS DRY AFTER APPLICATION USING SINGLE-SERVICE TOWELS TO AVOID CONTAMINATIN OF MILK.

POST-DIPPING: AFTER MILKING, SPRAY OR DIP ENTIRE TEAT WITH THIS PRODUCT. ALLOW TO AIR DRY.

NOTE: IF SOLUTION IN CUP BECOMES VISIBLY DIRTY, REPLENISH WITH A FRESH MIXTURE OF THIS PRODUCT. DO NOT RETURN UNUSED PRODUCT TO ORIGINAL CONTAINER.

Dermaplex PrePost JPN label (Revised 6/2/21)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dermaplex PrePost JPN label (Revised 6/2/21)

Dermaplex PrePost JPN label RevDermaplex PrePost JPN label Rev

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LACTIC ACID, UNSPECIFIED FORM Pharmacologic Class Indexing1Indexing - Pharmacologic Class20220121

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48106-2042-1Dermaplex PrePost JPN3902 g in 1 JUGLIQUID39022

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48106-2042DERMAPLEX PREPOST JPN (LACTIC ACID) LIQUID [BOUMATIC, LLC]21 package rows20210603_572ce09b-42fe-48e6-90b5-e2e65ddd00b8.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48106-204248106-2042-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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