Label: FAREWELL COLLECTION- antiseptic shower cream cream
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Contains inactivated NDC Code(s)
NDC Code(s): 81892-115-11 - Packager: Paveemol Company Limited
- 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 December 14, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- Do not use
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WHEN USING
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. - STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
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Inactive ingredients
acrylates copolymer, aloe barbadensis leaf extract, chlorphenesin, cocamidopropyl betaine, disodium EDTA, glycerin, glycol distearate, maltodextrin, phenoxyethanol, polyquaternium-7, propylene glycol, purified water USP, shea butter, sodium benzoate, sodium coco-sulfate, sodium laureth sulfate, triethanolamine.
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
FAREWELL COLLECTION
antiseptic shower cream creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81892-115 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.05 mg in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM LAURYL SULFATE (UNII: 368GB5141J) PHENOXYETHANOL (UNII: HIE492ZZ3T) CHLORPHENESIN (UNII: I670DAL4SZ) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) TROLAMINE (UNII: 9O3K93S3TK) SODIUM COCO-SULFATE (UNII: 3599J29ANH) POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y) ALOE VERA LEAF (UNII: ZY81Z83H0X) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) GLYCOL DISTEARATE (UNII: 13W7MDN21W) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) ACRYLATES CROSSPOLYMER-6 (UNII: 4GXD0Q3OS3) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) SODIUM BENZOATE (UNII: OJ245FE5EU) SHEA BUTTER (UNII: K49155WL9Y) MALTODEXTRIN (UNII: 7CVR7L4A2D) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81892-115-11 250 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 06/22/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 06/22/2021 Labeler - Paveemol Company Limited (660079138) Establishment Name Address ID/FEI Business Operations Paveemol Company Limited 660079138 manufacture(81892-115)