Label: BIOCELL- lactic acid liquid
- NDC Code(s): 55756-107-27
- Packager: DeLaval Inc.
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated May 2, 2016
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- WARNINGS AND PRECAUTIONS
- INDICATIONS & USAGE
- STORAGE AND HANDLING
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SPL UNCLASSIFIED SECTION
FIRST AID
Eye contact: Rinse eyes with plenty of water for at least 15 minutes. If irritation occurs, get medical attention.
Skin cntact: Wash with water. Get medical attention if irritation develops and persists.
If swallowed: DO NOT induce vomiting. Call a physician or poison control center immediately.
Inhalation: Move victim to fresh air. Get medical attention if symptoms persist.
- SPL UNCLASSIFIED SECTION
- SPL UNCLASSIFIED SECTION
- SPL UNCLASSIFIED SECTION
- SPL UNCLASSIFIED SECTION
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BIOCELL
lactic acid liquidProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:55756-107 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Lactic Acid (UNII: 33X04XA5AT) (Lactic Acid - UNII:33X04XA5AT) Lactic Acid 18.31 g in 1 L Inactive Ingredients Ingredient Name Strength C11-15 PARETH-20 (UNII: CW2175OSX0) POLYSORBATE 80 (UNII: 6OZP39ZG8H) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ALCOHOL (UNII: 3K9958V90M) ISOPROPYL ALCOHOL (UNII: ND2M416302) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) BRONOPOL (UNII: 6PU1E16C9W) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55756-107-27 1040.9 L in 1 DRUM Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/29/2012 Labeler - DeLaval Inc. (173704867) Registrant - DeLaval Inc. (173704867) Establishment Name Address ID/FEI Business Operations West Penetone Inc. 202373015 analysis, api manufacture, label, manufacture, pack