Label: CVS TRIPLE-THICK ANTIBACTERIAL WASHCLOTHS- benzalkonium chloride cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 59779-005-76 - Packager: CVS Pharmacy
- 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 September 24, 2015
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- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
Washcloths can be used at room temperature or heated in a microwave for extra comfort.
Heating instructions:
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- Place full package in microwave and heat for 45 seconds, then follow washing instructions
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- If heating a partial package (2 or more cloths), heat for 15 seconds and test temperature to avoid burning skin.
Washing instructions:
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- Gently pull label tab until package opening is exposed
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- Remove cloths one at a time to cleanse body parts in this order:
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- Face
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- Neck and abdomen
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- Right arm
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- Left arm
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- Right leg
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- Left leg
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- Back
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- Groin and buttocks
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- Allow skin to dry
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- Dispose of cloth in waste receptacle
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- Do not flush cloths in toilet
- Other information
- Inactive ingredients
- Package/Label Principal Display Panel
- Package Label - Drug Facts Box
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INGREDIENTS AND APPEARANCE
CVS TRIPLE-THICK ANTIBACTERIAL WASHCLOTHS
benzalkonium chloride clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.12 g in 100 mL Inactive Ingredients Ingredient Name Strength ALLANTOIN (UNII: 344S277G0Z) ALOE VERA LEAF (UNII: ZY81Z83H0X) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) EDETATE DISODIUM (UNII: 7FLD91C86K) LINOLEAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: 5Q87K461JO) POLYSORBATE 20 (UNII: 7T1F30V5YH) DIMETHICONE (UNII: 92RU3N3Y1O) SODIUM BENZOATE (UNII: OJ245FE5EU) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-005-76 8 in 1 PACKAGE 1 21 mL in 1 APPLICATOR; 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 part333A 11/01/2011 Labeler - CVS Pharmacy (062312574)