Label: BEARICAID ANTISEPTIC SKIN SANITIZING WIPES- ethyl alcohol cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 71504-659-01, 71504-659-58, 71504-659-66 - Packager: Knet Systems Corp.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated June 9, 2017
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Purpose
- Uses
- Warnings
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Inactive Ingredients
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SPL UNCLASSIFIED SECTION
Contains SkinscreenEx special blend with essential oils to support healthy skin
Use directly on the hands and skin to CLEAN, SANITIZE, and REDUCE bacteria that can potentially cause disease
Sanitizes and Cleans with HYGENIC GRADE EMBOSSED 6 X 6 CLOTH
RECOMMENDED SAFE FOR DAILY USE
50 INDIVIDUALLY SEALED PACKETS
Keeping hands clean is one of the best things you can do to keep from getting sick
Effectively Removes 99.99% of Germs AND Helps Reduce the Bacteria that can Potentially Cause Disease
EFFECTIVE AGAINST:
MRSA
STAPH
E.COLIALSO HELPS REDUCE E.COLI BACTERIA ASSOCIATED WITH THE FOLLOWING SYMPTOMS:
• PNEUMONIA
• EAR INFECTIONS
• BACTERIAL DIARRHEA
• URINARY TRACT
• INFECTIONS
• BACTERIAL (E.COLI) STOMACH FLU
• VOMITING
• FEVER
• NAUSEABearicaid does not contain triclosan, parabens, sulfates, or phthalates
Manufactured for: BEARICAID APPLIED SCIENCES
Los Angeles, CA 91331, Designed in USAMade in China
- Packaging
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INGREDIENTS AND APPEARANCE
BEARICAID ANTISEPTIC SKIN SANITIZING WIPES
ethyl alcohol clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71504-659 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 65.9 mL in 100 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) CHAMOMILE (UNII: FGL3685T2X) CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) TEA TREE OIL (UNII: VIF565UC2G) TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71504-659-01 3.48 mL in 1 PACKET; Type 0: Not a Combination Product 06/14/2017 2 NDC:71504-659-66 50 in 1 BOX 06/14/2017 2 3.48 mL in 1 PACKET; Type 0: Not a Combination Product 3 NDC:71504-659-58 150 in 1 BOX 06/14/2017 3 3.48 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 06/14/2017 Labeler - Knet Systems Corp. (092906539)