Label: BLACK ICE MEDICATED PATCHES- menthol patch
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Contains inactivated NDC Code(s)
NDC Code(s): 72411-102-01 - Packager: Carbon Biotech Llc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated July 16, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient (in each patch)
- Purpose
- Uses
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Warnings
For external use only
When using this product: • use only as directed • do not apply to wounds or damaged skin • avoid contact with eyes • do not bandage tightly
Stop use and ask a doctor if: condition worsens, or if symptoms persist for more than 7 days or 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 CHILDREN
- Directions
- Inactive ingredients
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SPL UNCLASSIFIED SECTION
HYDROGEL PATCH with ACTIVATED CHARCOAL
* helps relieve minor aches and pains of muscles and joints
* pain-relieving menthol on a breathable adhesive patch
* hydrogel infused with charcoal for smoother skin
* resealable pouch
* lasts up to 8 hours
VEGAN
No animal products or animal testing
For more info about charcoal and other free health resources, go to lifeandhealth.org
Distributed by Carbon Biotech LLC
110 Flocchini Circle, Ste 400
Lincoln, CA 95648
Made in China
- Packaging
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INGREDIENTS AND APPEARANCE
BLACK ICE MEDICATED PATCHES
menthol patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72411-102 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 0.156 g Inactive Ingredients Ingredient Name Strength ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) ALCOHOL (UNII: 3K9958V90M) BORNEOL (UNII: M89NIB437X) DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) DMDM HYDANTOIN (UNII: BYR0546TOW) GLYCERIN (UNII: PDC6A3C0OX) POVIDONE K30 (UNII: U725QWY32X) SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J) WATER (UNII: 059QF0KO0R) Product Characteristics Color black Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72411-102-01 1 in 1 PACKAGE; Type 0: Not a Combination Product 06/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 06/01/2018 Labeler - Carbon Biotech Llc (081166374)
