COLD HOT PATCH- menthol patch
cold hot patch by
Drug Labeling and Warnings
cold hot patch by is a Otc medication manufactured, distributed, or labeled by Zhejiang Bangli Medical Products CO.,LTD. Drug facts, warnings, and ingredients follow.
Drug Details [pdf]
- Active Ingredient
- Purpose
- Use
-
Warnning
For external use only.
When using this product.use only as directed . avoid contact with eyes and mucous membranes. do not apply to wounds or damaged skin.do not bandage tightly or use a heating pad
Stop use and ask doctor if
.excessive redness or irritation is present
.condition worsens
.pain persist for more than 7 days
.symptoms clear up and occur again within a few days
If pregnant or breast-feeding, ask a health professional before use, keep out of reach of childeren.If swallowed, get medical help or contact a poison control center right away. -
Directions
.adults and children 12 years and over: apply patch to affected area as needed but not more than 4 times daily
.children under 12 years: ask a doctor
. for easy application: grasp both ends of pad firmly, pull at both ends. Stretch pad until the backing separates.
Remove protective film while applying pad directly to site of pain. - Inactive Ingredients
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
COLD HOT PATCH
menthol patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 57900-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Menthol (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) Menthol 5 g in 100 g Inactive Ingredients Ingredient Name Strength Acrylic Acid (UNII: J94PBK7X8S) Aluminum Hydroxide (UNII: 5QB0T2IUN0) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) 2-ETHYLHEXYL ACRYLATE (UNII: HR49R9S6XG) Glycerin (UNII: PDC6A3C0OX) Isopropyl Myristate (UNII: 0RE8K4LNJS) Methyl Acrylate (UNII: WC487PR91H) NONOXYNOL-30 (UNII: JJX07DG188) SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L) POLYACRYLIC ACID (8000 MW) (UNII: 73861X4K5F) Polysorbate 80 (UNII: 6OZP39ZG8H) Sorbitan Sesquioleate (UNII: 0W8RRI5W5A) STARCH, POTATO (UNII: 8I089SAH3T) Talc (UNII: 7SEV7J4R1U) Tartaric Acid (UNII: W4888I119H) Titanium Dioxide (UNII: 15FIX9V2JP) Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 57900-002-01 4 in 1 CARTON 1 12 in 1 PACKAGE 1 1 in 1 BOX 1 2 in 1 BAG 1 0.408 g in 1 PATCH 2 NDC: 57900-002-02 3 in 1 CARTON 2 12 in 1 PACKAGE 2 6 in 1 BOX 2 1 in 1 BAG 2 0.408 g in 1 PATCH 3 NDC: 57900-002-03 4 in 1 CARTON 3 12 in 1 PACKAGE 3 1 in 1 BOX 3 3 in 1 BAG 3 0.408 g in 1 PATCH 4 NDC: 57900-002-04 50 in 1 CARTON 4 1 in 1 BOX 4 5 in 1 BAG 4 0.408 g in 1 PATCH 5 NDC: 57900-002-05 48 in 1 CARTON 5 3 in 1 BOX 5 1 in 1 BAG 5 0.408 g in 1 PATCH 6 NDC: 57900-002-06 8 in 1 CARTON 6 6 in 1 PACKAGE 6 1 in 1 BOX 6 5 in 1 BAG 6 0.408 g in 1 PATCH 7 NDC: 57900-002-07 4 in 1 CARTON 7 6 in 1 PACKAGE 7 1 in 1 BOX 7 5 in 1 BAG 7 0.408 g in 1 PATCH 8 NDC: 57900-002-08 4 in 1 CARTON 8 50 in 1 PACKAGE 8 1 in 1 BOX 8 5 in 1 BAG 8 0.85 g in 1 PATCH 9 NDC: 57900-002-09 30 in 1 CARTON 9 1 in 1 BOX 9 5 in 1 BAG 9 0.595 g in 1 PATCH 10 NDC: 57900-002-10 8 in 1 CARTON 10 6 in 1 PACKAGE 10 1 in 1 BOX 10 5 in 1 BAG 10 0.595 g in 1 PATCH 11 NDC: 57900-002-11 4 in 1 CARTON 11 6 in 1 PACKAGE 11 1 in 1 BOX 11 5 in 1 BAG 11 0.595 g in 1 PATCH 12 NDC: 57900-002-12 8 in 1 CARTON 12 6 in 1 PACKAGE 12 1 in 1 BOX 12 3 in 1 BAG 12 1.487 g in 1 PATCH Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 03/18/2014 Labeler - Zhejiang Bangli Medical Products CO.,LTD (421295875) Establishment Name Address ID/FEI Business Operations Zhejiang Bangli Medical Products CO.,LTD 421295875 manufacture(57900-002)
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.