Assured Pain Relief
- Dosage form
- GEL
- Labeler
- Foshan Aqua Gel Biotech Co., Ltd.,
- Label updated
- 2017-09-08
- Retrieved
- 2026-09-07
- Active ingredients
- LIDOCAINE
유효 성분
Active ingredients
Lidocaine 4%
성분·작용
Purpose
Topical analgesic
효능·용도
Uses temporarily releives minor pain
주의사항
Warnings for external use only.
Do not use
•more than one patch on your body at a time or on cut •on wounds or damaged skin •with a heating pad
When using this product
•avoid contact with eyes, mucous membranes or rashes •use only as directed •do not bandage tightly
•do not use at the same time as other topical analgesics •dispose of used patch in a manner that always keeps products away from children and pets
Stop use and ask a doctor if
•you experience signs of skin injury, such as pain, swelling or blistering where product was applied •symptoms persist for more than 7
days or clear up and occur again within a few days •condition worsens •redness is present •irritation develops
Label information
Keep out of reach of children. On case of accidental ingestion, get medical help or contact a Poison Control Center right away.
Label information
Pregnancy.breast-feeding warning. If pregant or breast-feeding, ask a health professional before use.
복용법·사용법
Directions Adults and children 12 years of age and over:
•Clean and dry affected area •Remove film from patch and apply to the skin (see package for instructions)
•Apply to affected area not more than 3 to 4 times daily •Remove patch from the skin after at most 8 hours of application
Children under 12 years of age: consult a physician
보관·기타 정보
Other information
•Store at room temperature 58° - 86° F (15° - 30° C). Acoid storing product in direct sunlight •Protect product from excessive moisture
첨가제
Inactive ingredients DIHYDROXYALUMINUM AMINOACETATE, GLYCERIN, KAOLIN, METHYLPARABEN, PROPYLPARABEN, PROPYLENE GLYCOL,
PVP, POLYACRYLIC ACID, POLYSORBATE 80, SODIUM POLYACRYLATE, TITANIUM DIOXIDE, TARTARIC ACID, WATER
포장 표시
[Image in the official label — see DailyMed source]
DailyMed Set ID: bdbd4106-e4fe-4daf-a757-3aee3a87bb09 · Version 2
NDC: 69159-100