Label: DERMAPLEX PREPOST JPN- lactic acid liquid
- NDC Code(s): 48106-2042-1
- Packager: BouMatic, LLC
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated May 26, 2021
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
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USE DIRECTIONS
NOT FOR HUMAN USE
FOR EXTERNAL USE ONLY
USE AT FULL STRENGTHFIRST 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:
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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)
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INGREDIENTS AND APPEARANCE
DERMAPLEX PREPOST JPN
lactic acid liquidProduct 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
