Label: TRIPLE SHIELD- benzalkonium chloride spray
- NDC Code(s): 71884-034-16
- Packager: Enviro Specialty Chemicals Inc
- 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 August 26, 2020
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- DRUG FACTS
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- WARNINGS
- INACTIVE INGREDIENT
- QUESTIONS
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SPL UNCLASSIFIED SECTION
FAST ACTING
15-SECOND FORMULA
WITH SOOTHING
ALOE VERA
Long lasting, sanitizing protection from germs for the entire body
KILLS 99.99% OF GERMS
Formulated and enhanced with
Zetrisil®
DISTRIBUTED BY TRIPLEROOT®
10004 WURZBACH RD. #104
SAN ANTONIO, TX 78230
www.tripleshieldusa.com
sales@tripleroot.com
FORMULATED IN THE USA | MADE IN CHINA
- Packaging
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INGREDIENTS AND APPEARANCE
TRIPLE SHIELD
benzalkonium chloride sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71884-034 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.10 g in 100 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) LAURETH-4 (UNII: 6HQ855798J) PHENOXYETHANOL (UNII: HIE492ZZ3T) TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDE (UNII: XGN40YQC7B) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71884-034-16 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/26/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 08/26/2020 Labeler - Enviro Specialty Chemicals Inc (202621850)