Label: CHEMSTATION Q E2- benzalkonium chloride liquid
- NDC Code(s): 71212-102-00, 71212-102-01, 71212-102-02
- Packager: Chemstation
- 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 January 2, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- QUESTIONS
-
OTHER SAFETY INFORMATION
Can cause eye irritation
Response:
IF IN EYES: Contact may cause mild, transient irritation. For irritation, rinse cautiously with water for several minutes.
Remove contact lenses, if present and easy to do. Continue rinsing. If eye irritation persists, get medical advice/attention.
IF ON SKIN (or hair): Not expected to be irritating, sensitizing, photoallerginic or phototoxic when used as intended. If irritation occurs following intended use or prolonged contact, it is expected to be mild and transient.
Storage: Store in a dry area at normal temperatures.
Disposal: Dispose of contents/container to an approved waste disposal plant.
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CHEMSTATION Q E2
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71212-102 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.2 g in 1 L Inactive Ingredients Ingredient Name Strength CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) BENZYL ALCOHOL (UNII: LKG8494WBH) PHENOXYETHANOL (UNII: HIE492ZZ3T) EDETIC ACID (UNII: 9G34HU7RV0) DEHYDROACETIC ACID (UNII: 2KAG279R6R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71212-102-02 6 in 1 BOX 03/08/2017 1 1.25 L in 1 CARTRIDGE; Type 0: Not a Combination Product 2 NDC:71212-102-01 4 in 1 BOX 03/08/2017 2 3.79 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 3 NDC:71212-102-00 208.198 L in 1 DRUM; Type 0: Not a Combination Product 03/08/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 03/08/2017 Labeler - Chemstation (177350279)