Label: SKIN PROTECTANT FLUSHABLE WIPES- dimethicone liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 44019-004-00 - Packager: Yinjing Medical Technology (Shanghai) Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
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 December 27, 2017
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Skin Protectant Flushable Wipes
- Active Ingredient
- Purpose
- Use
- Warnings
- Directions
- Other Information
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Inactive Ingredients
WATER, SODIUM COCO PG-DIMONIUM CHLORIDE PHOSPHATE, LINOLEAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE, POLYSORBATE-20, DISODIUM EDTA, CETEARYL ISONONANOATE, CETEARETH-20, CETEARYL ALCOHOL, GLYCERYL STEARATE, CETEARETH-12, CETYL PALMITATE, GLYCERIN, SODIUM BENZOATE, BENZALKONIUM CHLORIDE, PHENOXYETHANOL, ALOE VERA LEAF JUICE, CITRIC ACID
- Skin Protectant Flushable Wipes 24 Wipes (44019-004-00)
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INGREDIENTS AND APPEARANCE
SKIN PROTECTANT FLUSHABLE WIPES
dimethicone liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:44019-004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 3.2 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) LINOLEAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: 5Q87K461JO) POLYSORBATE 20 (UNII: 7T1F30V5YH) EDETATE DISODIUM (UNII: 7FLD91C86K) CETEARYL ISONONANOATE (UNII: P5O01U99NI) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) CETEARETH-12 (UNII: 7V4MR24V5P) CETYL PALMITATE (UNII: 5ZA2S6B08X) GLYCERIN (UNII: PDC6A3C0OX) SODIUM BENZOATE (UNII: OJ245FE5EU) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) PHENOXYETHANOL (UNII: HIE492ZZ3T) ALOE VERA LEAF (UNII: ZY81Z83H0X) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:44019-004-00 24 in 1 BAG 08/03/2016 1 12.33 g in 1 PATCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 08/03/2016 Labeler - Yinjing Medical Technology (Shanghai) Co., Ltd. (530501535) Registrant - Yinjing Medical Technology (Shanghai) Co., Ltd. (530501535)