![WELLAGE DEEP LAYER SILKY FACIAL OIL (SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, ARGANIA SPINOSA KERNEL OIL, LIMNANTHES ALBA (MEADOWFOAM) SEED OIL, SQUALANE) OIL [HUGEL PHARMA CO.,LTD]](https://medic.hrt.org//dailymed/images/3bf54d7e-473a-24d8-e054-00144ff88e88/l.jpg)
| NDC | 69346-0005-1 |
| Set ID | 3bf54d7e-473a-24d8-e054-00144ff88e88 |
| Category | HUMAN OTC DRUG LABEL |
| Packager | HUGEL PHARMA CO.,LTD |
| Generic Name | |
| Product Class | |
| Product Number | |
| Application Number |
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
・Stop using the product when you have skin problems or the product disagrees with your skin
・Stop using the product immediately and consult a dermatologist if you have redness, swelling, itching or irritation on the skin while or after using the product.
・If the product gets into the eyes, don't rub but rinse with water.
・Don't place the product in any place where it will be subjected to extremely high or low temperatures or direct sunlight. - DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
WELLAGE DEEP LAYER SILKY FACIAL OIL
simmondsia chinensis (jojoba) seed oil, argania spinosa kernel oil, limnanthes alba (meadowfoam) seed oil, squalane oilProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69346-0005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y) (MEADOWFOAM SEED OIL - UNII:412ZHA4T4Y) MEADOWFOAM SEED OIL 6 g in 100 mL SQUALANE (UNII: GW89575KF9) (SQUALANE - UNII:GW89575KF9) SQUALANE 6 g in 100 mL ARGAN OIL (UNII: 4V59G5UW9X) (ARGAN OIL - UNII:4V59G5UW9X) ARGAN OIL 15 g in 100 mL SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H) (SIMMONDSIA CHINENSIS SEED - UNII:D24K2Q1F6H) SIMMONDSIA CHINENSIS SEED 35.1995 g in 100 mL Inactive Ingredients Ingredient Name Strength BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69346-0005-1 40 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 05/01/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/01/2016 Labeler - HUGEL PHARMA CO.,LTD (688400184) Registrant - HUGEL PHARMA CO.,LTD (688400184) Establishment Name Address ID/FEI Business Operations HUGEL PHARMA CO.,LTD 688400184 manufacture(69346-0005)
