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Body Essence Raspberry Antibacterial

Medically reviewed on Jan 22, 2018

Dosage form: lotion
Ingredients: TRICLOSAN 1.7uL in 1mL
Labeler: PureTek Corporation
NDC Code: 59088-740

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.

Triclosan 0.17%

Antibacterial moisturizing hand lotion.

Caution: Keep out of reach of children. For external use only. If swallowed, get medical help or contact a Poison Control Center immediately.

Helps kill germs and keep them away.

Do not use on or near eyes. In case of contact, rinse eyes thoroughly with water. If irritation or redness develops, discontinue use.

Directions: Dispense lotion onto hands and rub into skin until absorbed.

INACTIVE INGREDIENTS: PURIFIED WATER, STEARIC ACID, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, CETYL ALCOHOL, C12-15 ALKYL ETHYLHEXANOATE, DIMETHICONE, MENTHYL LACTATE, RETINYL PALMITATE (VITAMIN A), TOCOPHERYL ACETATE (VITAMIN E), PANTHENOL (PROVITAMIN B5), CAMELLIA OLEIFERA SEED EXTRACT (WHITE TEA AND OOLONG TEA), CAMELLIA SINENSIS (GREEN TEA) LEAF EXTRACT, TRITICUM VULGARE (WHEAT) GERM OIL, HYDROLYZED SILK, LACTOSE, LAURETH-7, GLYCERYL STEARATE, PEG-100 STEARATE, CETYL PHOSPHATE, HYDROXYPROPYL METHYLCELLULOSE, BUTYLENE GLYCOL, C13-14 ISOPARAFFIN, NYLON-12, POLYACRYLAMIDE, CARBOMER, BHT, TRIETHANOLAMINE, PHENOXYETHANOL, BUTYLPARABEN, ETHYLPARABEN, ISOBUTYLPARABEN, METHYLPARABEN, PROPYLPARABEN, FRAGRANCE, RED 4 (CI 14700), ULTRAMARINES (CI 77007), XANTHAN GUM, YELLOW 6 (CI 15985).

THIS PRODUCT CONTAINS NATURAL INGREDIENTS, WHICH MAY CAUSE COLOR VARIATION.

BODY ESSENCE RASPBERRY ANTIBACTERIAL  
triclosan lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59088-740
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (TRICLOSAN) TRICLOSAN1.7 uL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
STEARIC ACID 
SUNFLOWER OIL 
CETYL ALCOHOL 
DIMETHICONE 
MENTHYL LACTATE 
VITAMIN A PALMITATE 
.ALPHA.-TOCOPHEROL ACETATE, DL- 
PANTHENOL 
CAMELLIA OLEIFERA SEED 
GREEN TEA LEAF 
WHEAT GERM OIL 
LACTOSE 
LAURETH-7 
GLYCERYL MONOSTEARATE 
POLYOXYL 100 STEARATE 
CETYL PHOSPHATE 
HYPROMELLOSES 
BUTYLENE GLYCOL 
C13-14 ISOPARAFFIN 
CARBOMER HOMOPOLYMER TYPE A 
BUTYLATED HYDROXYTOLUENE 
TROLAMINE 
PHENOXYETHANOL 
BUTYLPARABEN 
ETHYLPARABEN 
ISOBUTYLPARABEN 
METHYLPARABEN 
PROPYLPARABEN 
FD&C RED NO. 4 
XANTHAN GUM 
FD&C YELLOW NO. 6 
Packaging
#Item CodePackage Description
1NDC:59088-740-0559 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A12/28/2009
Labeler - PureTek Corporation (785961046)
Establishment
NameAddressID/FEIOperations
PureTek Corporation785961046manufacture, label, pack, outsourcing human drug compounding, relabel, repack
Establishment
NameAddressID/FEIOperations
PureTek Corporation031678746manufacture, pack, label, outsourcing human drug compounding, repack, relabel

 
PureTek Corporation

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