DERMABLEND- lactic acid concentrate

DERMABLEND by

Drug Labeling and Warnings

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

Drug Details [pdf]

INDICATIONS & USAGE

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TEAT DIP CONCENTRATE

Helps reduce the spread of organisms which may cause Mastitis

USE DIRECTIONS

NOT FOR HUMAN USE

FOR EXTERNAL USE ONLY

USE ONLY AS DIRECTED

Do not use in concentrated form.
Must dilute prior to use.

To obtain a 0.5% Lactic Acid, 0.21%
DDBSA solution and 2.% emollients,
add 1 part DermaBlend to 9 parts water
and mix thoroughly.

Active Ingredient (Lactic Acid 5%,
DDBSA 2.0%)
Emollients (Glycerin 20%)

PRECAUTIONS

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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

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INGREDIENTS AND APPEARANCE

DERMABLEND 
lactic acid concentrate

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 48106-1316
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LACTIC ACID (UNII: 33X04XA5AT) (LACTIC ACID - UNII:33X04XA5AT)	LACTIC ACID	50 g  in 1 L
DODECYLBENZENESULFONIC ACID (UNII: 60NSK897G9) (DODECYLBENZENESULFONIC ACID - UNII:60NSK897G9)	DODECYLBENZENESULFONIC ACID	20 g  in 1 L

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48106-1316-5	208 L in 1 DRUM
2	NDC: 48106-1316-6	1040 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK
3	NDC: 48106-1316-1	3.8 L in 1 DRUM
4	NDC: 48106-1316-2	18.9 L in 1 DRUM
5	NDC: 48106-1316-3	56.8 L in 1 DRUM
6	NDC: 48106-1316-4	114 L in 1 DRUM

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		01/01/2015

Labeler - BouMatic, LLC (124727400)

Registrant - BouMatic, LLC (124727400)

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

Establishment
Name	Address	ID/FEI	Business Operations
Knapp Manufacturing		063012827	api manufacture, manufacture