- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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WARNINGS
1. If the following symptoms occur after product use, stop using the product immediately and consult a dermatologist (continuous use can exacerbate the symptoms).
1) Occurrence of red spots, swelling, itchiness, and other skin irritation
2) If the symptoms above occur after the application area is exposed to direct sunlight2. Do not use on open wounds, eczema, and other skin irritations
3. Precaution for Storage and Handling
1) Close the lid after use
2) Keep out of reach of infants and children
3) Do not to store in a place with high/low temperature and exposed to direct sunlight4. Use as avoiding eye areas.
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INDICATIONS & USAGE
- Wash hair with the Scalp Scaling Shampoo and dry thoroughly.
- Use blow-dryer’s cool air function to dry hair - On a dry scalp, apply the Synergy Booster by tapping gently on the area (15 to 20 times).
- The Synergy Booster being sprayed directly from the container nozzles, its scalp penetrability is very high and, combined with scalp stimulation through massaging and blood circulation activation, absorption rates get higher. - Tap and press on the scalp using finger.
- After using Synergy Booster, make sure that all the topical solution is absorbed by gently tapping on the scalp.
- Wash hair with the Scalp Scaling Shampoo and dry thoroughly.
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SYNERGY BOOSTER
panthenol, salicylic acid, menthol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71175-0002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.25 g in 100 mL PANTHENOL (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z) PANTHENOL 0.2 g in 100 mL MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.3 g in 100 mL Inactive Ingredients Ingredient Name Strength BUTYLENE GLYCOL (UNII: 3XUS85K0RA) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71175-0002-1 100 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 01/11/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/10/2017 Labeler - zaol (689851635) Registrant - zaol (689851635) Establishment Name Address ID/FEI Business Operations zaol 689851635 pack(71175-0002) , manufacture(71175-0002) , label(71175-0002)