DERMAPLEX PREPOST JPN- lactic acid liquid

Dermaplex PrePost JPN by

Drug Labeling and Warnings

Dermaplex PrePost JPN by is a Animal medication manufactured, distributed, or labeled by BouMatic, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

USE DIRECTIONS

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:

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

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)

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

INGREDIENTS AND APPEARANCE

DERMAPLEX PREPOST JPN 
lactic acid liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 48106-2042
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LACTIC ACID (UNII: 33X04XA5AT) (LACTIC ACID - UNII:33X04XA5AT)	LACTIC ACID	5.68 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	85.82 g  in 100 g
SORBITOL (UNII: 506T60A25R)	2 g  in 100 g
GLYCERIN (UNII: PDC6A3C0OX)	3 g  in 100 g
DODECYL BENZENE SULFONATE DIETHANOLAMINE (MIXED ISOMERS) (UNII: 3WAK1N1OZ5)	1.5 g  in 100 g
SODIUM HYDROXIDE (UNII: 55X04QC32I)	2 g  in 100 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48106-2042-1	3902 g in 1 JUG

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/31/2021

Labeler - BouMatic, LLC (124727400)

Establishment
Name	Address	ID/FEI	Business Operations
BouMatic, LLC		124727400	api manufacture