Label: GIANT EAGLE COCONUT WATER FOAMING- benalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 63148-842-07 - Packager: Apollo Health and Beauty Care
- 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 November 4, 2016
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- Active ingredient
- Uses
- Warnings
- Directions
- Other information
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Inactive ingredients
Water (Aqua), Cocamidopropyl Betaine, Polysorbate 20, Glycerin, Fragrance (Parfum), Sodium Citrate, Xanthan Gum, Decyl Glucoside, Polyquaternium-7, Tetrasodium EDTA, Citric Acid, Cocos Nucifera (Coconut) Fruit Extract, Bambusa Vulgaris Leaf Extract, Aloe Barbadensis Leaf Juice, Methychloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI 42090), Red 33 (CI 17200).
- Label Copy
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INGREDIENTS AND APPEARANCE
GIANT EAGLE COCONUT WATER FOAMING
benalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63148-842 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) POLYSORBATE 20 (UNII: 7T1F30V5YH) GLYCERIN (UNII: PDC6A3C0OX) SODIUM CITRATE (UNII: 1Q73Q2JULR) XANTHAN GUM (UNII: TTV12P4NEE) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y) EDETATE SODIUM (UNII: MP1J8420LU) COCONUT (UNII: 3RT3536DHY) BAMBUSA VULGARIS LEAF (UNII: EMY54R518C) ALOE VERA LEAF (UNII: ZY81Z83H0X) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) D&C RED NO. 33 (UNII: 9DBA0SBB0L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63148-842-07 222 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/03/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 11/03/2016 Labeler - Apollo Health and Beauty Care (201901209) Registrant - Apollo Health and Beauty Care (201901209) Establishment Name Address ID/FEI Business Operations Apollo Health and Beauty Care 201901209 manufacture(63148-842)