DERMAPLEX- lactic acid liquid

Dermaplex by

Drug Labeling and Warnings

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

Drug Details [pdf]

INDICATIONS & USAGE

NON-IODINE BARRIER POST TEAT DIP

Helps reduce the spread of organisms which may cause Mastitis

USE DIRECTIONS

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

POST-DIPPING: After milking, 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.

Active Ingredient (Lactic Acid 5%)
Emollients 5%

PRECAUTIONS

CAUTION

KEEP OUT OF REACH OF CHILDREN
NOT FOR HUMAN USE

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.

PRECAUTION: Avoid eye contact. Do not ingest. Do not mix with any chemicals except as directed.

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

SEE MATERIAL SAFETY DATA SHEET

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DERMAPLEX 
lactic acid liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 48106-1167
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LACTIC ACID (UNII: 33X04XA5AT) (LACTIC ACID - UNII:33X04XA5AT)	LACTIC ACID	500 mL  in 10 L

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48106-1167-1	3.8 L in 1 DRUM
2	NDC: 48106-1167-2	18.9 L in 1 DRUM
3	NDC: 48106-1167-3	56.8 L in 1 DRUM
4	NDC: 48106-1167-7	114 L in 1 DRUM
5	NDC: 48106-1167-5	208 L in 1 DRUM
6	NDC: 48106-1167-6	1040 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		08/01/2007

Labeler - BouMatic, LLC (124727400)

Registrant - BouMatic, LLC (124727400)

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