NDC | 68233-804-01 |
Set ID | a2d5ae44-1510-422c-9334-e0381eef2824 |
Category | HUMAN OTC DRUG LABEL |
Packager | Albert Max, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART348 |
- Drug Facts
- Active Ingredients
- Purpose
- Uses
-
Warnings
For external use only
Do not use
•on wounds •irritated or damaged skin •sensitive skin
•with a heating pad •if pregnant
•with, or as the same time as, other external analgesic products
•if allergic to aspirin or salicylates
•if allergic to any ingredients of this product
When using this product
•avoid contact with the eyes
•do not bandage tightly
•do not apply to wounds or damaged skin
•do not use more than 3 plasters a day
•do not use 1 hour before or after bathing
Stop use and ask a doctor if
•condition worsens
•symptoms persist for more than 7 days
•symptoms clear up and occur again within a few days
•excessive irritation of the skin develops
•rashes, itching or redness are present
•side effects occur.
If pregnant, ask a health professional before use. - KEEP OUT OF REACH OF CHILDREN
-
Directions
•Adults and children 12 years of age and older: clean and dry affected area. Remove plaster from the protective layer, apply to the affected area, rub the area with your hand to secure the patch.
•Plaster will remain effective for 8 hours.
•Avoid using the same patch on the same area for more than 2 days.
•Do not apply to area with excessive hair. Adhesive plaster may hurt skin upon removal.
•Wet patch with warm water before removing from skin
•Children under 12 years of age: Do not use or consult a doctor. - Other Information
- Inactive ingredients
- QUESTIONS
- SPL UNCLASSIFIED SECTION
- Packaging
-
INGREDIENTS AND APPEARANCE
ZHONG HUA FENG SHI DIE DA GAO EXTERNAL ANALGESIC PLASTER
menthol, methyl salicylate patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68233-804 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM 0.04 g in 1 g METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 0.01 g in 1 g Inactive Ingredients Ingredient Name Strength CLEMATIS CHINENSIS ROOT (UNII: 8Z18N528CU) YELLOW WAX (UNII: 2ZA36H0S2V) MOMORDICA COCHINCHINENSIS SEED (UNII: 2T87O1UPVD) RICINUS COMMUNIS SEED (UNII: 7EK4SFN1TX) MYRRH (UNII: JC71GJ1F3L) FRANKINCENSE (UNII: R9XLF1R1WM) SESAME OIL (UNII: QX10HYY4QV) PINUS MASSONIANA RESIN (UNII: 64S07U83T7) FD&C BLUE NO. 2 (UNII: L06K8R7DQK) YELLOW OB (UNII: QE535CBH7S) ZINC OXIDE (UNII: SOI2LOH54Z) Product Characteristics Color green Score Shape RECTANGLE Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68233-804-01 5 in 1 BAG 11/01/2005 1 1.7 g in 1 PATCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 11/01/2005 Labeler - Albert Max, Inc. (149445798)