NDC | 55878-105-22, 55878-105-24, 55878-105-54 |
Set ID | 62caa4a8-e7b0-4a2e-824b-861652a240ee |
Category | HUMAN OTC DRUG LABEL |
Packager | Halogent, LLC (DBA Exposed Skin Care) |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333D |
- PURPOSE
- ACTIVE INGREDIENT
- WARNINGS
- INDICATIONS & USAGE
- ASK DOCTOR/PHARMACIST
- KEEP OUT OF REACH OF CHILDREN
- WHEN USING
-
DOSAGE & ADMINISTRATION
Directions
Wet your face and gently massage facial cleanser into skin for 10 - 15 seconds, avoiding contact with eyes. Thoroughly rinse your face with lukewarm water.
- Wash the entire affected area one to three times daily.
- Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
- If bothersome dryness or peeling occurs, reduce application to once a day or every other day.
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
FACIAL CLEANSER
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55878-105 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.5 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SODIUM C18 OLEFIN SULFONATE (UNII: Z6CI2A44YH) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) TROLAMINE (UNII: 9O3K93S3TK) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y) PANTHENOL (UNII: WV9CM0O67Z) PHENOXYETHANOL (UNII: HIE492ZZ3T) EDETATE DISODIUM (UNII: 7FLD91C86K) SALVIA OFFICINALIS FLOWERING TOP (UNII: 48JCS720FN) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55878-105-54 1 in 1 BOX 1 NDC:55878-105-24 120 mL in 1 BOTTLE 2 NDC:55878-105-22 60 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 02/07/2013 Labeler - Halogent, LLC (DBA Exposed Skin Care) (790961697)