Label: PREPARING TONIC- salicylic acid lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 51830-054-07 - Packager: Lange SAS
- 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 February 12, 2013
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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INDICATIONS & USAGE
PREPARING TONIC LOTION LANGE
LANGE Tonic Lotion will help to minimise pore size with its astringent ingredients and boost sebum regulation with its Zinc PCA extracts. Its Salicylic Acid limits bacterial growht and Stinging Nettle extract is antiseptic and Anti-Inflammatory. Skin is smoother and complexion is brighter with Tonic Lotion main actions:
Clears away dead cells,
Prevents blackheads formation,
Absorbs the excess of sebum. - WARNINGS
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
WATER
PROPYLENE GLYCOL
URTICA DIOICA EXTRACT
SORBITOL
PHENOXYETHANOL
METHYLPARABEN
ETHYLPARABEN
BUTYLPARABEN
PROPYLPARABEN
ISOBUTYLPARABEN
SODIUM LACTATE
ZINC PCA
POLYSORBATE 80
BENZYL ALCOHOL
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
TRIETHYLENE GLYCOL
MAGNESIUM NITRATE
MAGNESIUM CHLORIDE
TETRASODIUM EDTA
SALICYLIC ACID
PANTHENOL
ALLANTOIN
YELLOW FIVE
ALCOHOL DENAT.
IMIDAZOLIDINYL UREA
CITRIC ACID - PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PREPARING TONIC
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51830-054 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 1.8 mg in 180 mg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SORBITOL (UNII: 506T60A25R) PHENOXYETHANOL (UNII: HIE492ZZ3T) METHYLPARABEN (UNII: A2I8C7HI9T) ETHYLPARABEN (UNII: 14255EXE39) PROPYLPARABEN (UNII: Z8IX2SC1OH) BUTYLPARABEN (UNII: 3QPI1U3FV8) ISOBUTYLPARABEN (UNII: 0QQJ25X58G) SODIUM LACTATE (UNII: TU7HW0W0QT) POLYSORBATE 80 (UNII: 6OZP39ZG8H) BENZYL ALCOHOL (UNII: LKG8494WBH) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) TRIETHYLENE GLYCOL (UNII: 3P5SU53360) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) MAGNESIUM NITRATE (UNII: 77CBG3UN78) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) EDETATE SODIUM (UNII: MP1J8420LU) METHYLPARABEN SODIUM (UNII: CR6K9C2NHK) PANTHENOL (UNII: WV9CM0O67Z) ALLANTOIN (UNII: 344S277G0Z) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) IMIDUREA (UNII: M629807ATL) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) ZINC PIDOLATE (UNII: C32PQ86DH4) ALCOHOL (UNII: 3K9958V90M) URTICA DIOICA LEAF (UNII: X6M0DRN46Q) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51830-054-07 180 mg in 1 BOX Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333D 07/18/2012 Labeler - Lange SAS (275956105) Establishment Name Address ID/FEI Business Operations Lange SAS 275956105 manufacture(51830-054)
