NDC | 63868-249-07 |
Set ID | 91dcaea1-bb34-484b-9798-94dd4e0aa49b |
Category | HUMAN OTC DRUG LABEL |
Packager | Chain Drug Marketing Association |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333D |
- Active ingredient
- Purpose
- Indications
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Warnings
For external use only.
Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.
When using this product avoid contact with the eyes. If product gets into eyes, rinse thoroughly with water.
- Keep Out of Reach of Children.
- Directions
- Other Information
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Inactive ingredients
water, glycerin, sodium lauroyl sarcosinate, stearic acid, potassium hydroxide, myristic acid, lauric acid, palmitic acid, fragrance, phenoxyethanol, ethylhexylglycerin, polyquaternium-10, disodium EDTA, methylparaben, ethylparaben, butylparaben, propylparaben, isobutylparaben, aloe barbadensis leaf juice, sodium benzoate, potassium sorbate, menthol.
- Package/Label Principal Display Panel Awaken by Quality Choice® oil-free daily face wash Acne Fighting Medication Salicylic acid Fewer breakouts in just 4 weeks Non-drying *Compare to Clearasil Ultra® Daily Face Wash ingredients Net Wt 6.5 Fl Oz (184 mL) Distributed by C.D.M.A., Inc.® 43157 W. Nine MileNovi, MI 48376-0995 Questions: 248-449-9300*This product is not manufactured or distributed by Reckitt Benckiser owner of the registered trademark Clearasil Daily Clear®.Manufactured in Israel0D48A CD T1
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INGREDIENTS AND APPEARANCE
AWAKEN OIL-FREE DAILY FACE WASH
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-249 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618) STEARIC ACID (UNII: 4ELV7Z65AP) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) MYRISTIC ACID (UNII: 0I3V7S25AW) LAURIC ACID (UNII: 1160N9NU9U) PALMITIC ACID (UNII: 2V16EO95H1) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK) EDETATE DISODIUM (UNII: 7FLD91C86K) METHYLPARABEN (UNII: A2I8C7HI9T) ETHYLPARABEN (UNII: 14255EXE39) BUTYLPARABEN (UNII: 3QPI1U3FV8) PROPYLPARABEN (UNII: Z8IX2SC1OH) ISOBUTYLPARABEN (UNII: 0QQJ25X58G) ALOE VERA LEAF (UNII: ZY81Z83H0X) SODIUM BENZOATE (UNII: OJ245FE5EU) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) MENTHOL (UNII: L7T10EIP3A) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63868-249-07 184 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 09/01/2014 Labeler - Chain Drug Marketing Association (011920774)