OXYBLEND
- Manufacturer
- BouMatic, LLC
- Effective date
- 2012-01-01
- Label type
- OTC ANIMAL DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-06-01 02:39:25
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
HYDROGEN PEROXIDE TEAT DIP CONCENTRATE
Helps reduce the spread of organisms which may cause Mastitis.
USE DIRECTIONS
NOT FOR HUMAN USE
FOR EXTERNAL USE ONLY
Do not use in concentrated form.
Must dilute prior to use.
To obtain a 1% hydrogen peroxide solution and 2% emollients, add 1 part OxyBlend LE to 4 parts water and mix thoroughly.
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 a 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
Emergency No. Only/No. d'urgence Seulement/No. de Emergencia Solo:
US/CANADA only (1-800-255-3924) (ChemTel, Inc)
International (+01-813-248-0585) (ChemTel, Inc)
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
OxyBlend LE Label
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48106-1187-5 | OXYBLENDLE | 208 L in 1 DRUM | LIQUID | 208 | 4 | |
| 48106-1187-6 | OXYBLENDLE | 1040 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK | LIQUID | 1040 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48106-1187 | OXYBLEND LE (HYDROGEN PEROXIDE) LIQUID [BOUMATIC, LLC] | 4 | 2 package rows | 20120217_bfe9dcec-5204-49a7-a2fb-fe6a8bc67c5b.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| HYDROGEN PEROXIDE | ACTIVE INGREDIENT | BBX060AN9V | 4 | |
| HYDROGEN PEROXIDE | ACTIVE MOIETY | BBX060AN9V | 4 |
Products#
Every source-derived product name is available through these pages.
- OXYBLEND LE
- HYDROGEN PEROXIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48106-1187 | 48106-1187-5, 48106-1187-6 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| HYDROGEN PEROXIDE | BBX060AN9V | ACTIB |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
