Label: SKIN AID MEDICS ANTIBACTERIAL ALOE VERA CREAMY- benzalkonium chloride 0.13% liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 73166-108-16 - Packager: Larry (Xiamen) Hi Tech Co., Ltd
- 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 17, 2020
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor
- Keep out of reach of children.
- Directions
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Inactive Ingredients
Aqua Water, sodium laureth sulfate, cocoamidopropyl betaine, sodium chloride, glycerin, glycol distearate parfum, PEG-150 Distearate, Aloe Barbadensis Leaf Juice, Disodium EDTA, Methylchloroisothiazolinone, Methylisothazolinone, magnesium chloride, Magnesium Nitrate, Citric Acid, Tocopheryl Acetate, Food Yellow 4 (CI 19140) Food Blue 2 (CI 42090)
- Questions or Comments?
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INGREDIENTS AND APPEARANCE
SKIN AID MEDICS ANTIBACTERIAL ALOE VERA CREAMY
benzalkonium chloride 0.13% liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73166-108 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.65 g in 500 mL Inactive Ingredients Ingredient Name Strength GLYCOL DISTEARATE (UNII: 13W7MDN21W) ALOE VERA LEAF (UNII: ZY81Z83H0X) MAGNESIUM NITRATE (UNII: 77CBG3UN78) MAGNESIUM CHLORIDE ANHYDROUS (UNII: 59XN63C8VM) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) GLYCERIN (UNII: PDC6A3C0OX) POLYETHYLENE GLYCOL 100000 (UNII: V46Y6OJ5QB) SODIUM CHLORIDE (UNII: 451W47IQ8X) WATER (UNII: 059QF0KO0R) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) DISODIUM EDTA-COPPER (UNII: 6V475AX06U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73166-108-16 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/01/2020 Labeler - Larry (Xiamen) Hi Tech Co., Ltd (529759328) Registrant - G2 Beauty Inc (124608169)