Label: DERMAPLEX PRE-POST- lactic acid liquid
48106-1183-4, view more48106-1183-5, 48106-1183-6
- 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.
Updated January 1, 2012
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INDICATIONS & USAGE
TEAT DIP AND/OR TEAT SPRAYHelps reduce the spread of organisms which may cause Mastitis
NOT FOR HUMAN USE
FOR EXTERNAL USE ONLY
USE AT FULL STRENGTH
PRE-DIPPING: Before milking, dip or spray entire teat with this product. Wipe teats dry after application using single-service towels to avoid contamination 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.
Active Ingredient (Lactic Acid 5%)
KEEP OUT OF REACH OF CHILDREN
NOT FOR HUMAN USE
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
lactic acid liquid
Product Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:48106-1183 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:48106-1183-1 3.8 L in 1 DRUM 2 NDC:48106-1183-2 18.9 L in 1 DRUM 3 NDC:48106-1183-3 56.8 L in 1 DRUM 4 NDC:48106-1183-4 114 L in 1 DRUM 5 NDC:48106-1183-5 208 L in 1 DRUM 6 NDC:48106-1183-6 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