Label: MD SCIENCE CANNABIDIOL- lidocaine and histamine dihydrochloride cream
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Contains inactivated NDC Code(s)
NDC Code(s): 73615-103-03 - Packager: MD NATURAL HEALTH 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 February 10, 2020
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Use
- Warnings
- Directions
- Other Information
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Inactive Ingredients
Aloe Barbadensis (Aloe)Leaf Juice, Caprylhydroxamic Acid, Caprylyl Glycol, Carbomer, CBD (Cannabidiol), Cetyl Esters, Cocos Nucifera (Coconut) Oil, Emu Oil, Glycerin, Glyceryl Stearate, Isopropyl Palmitate, Methylsulfonylmethane (MSM), Sodium Hydroxide, Sorbitol, Steareth-21, Stearyl Alcohol, Water.
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 88 ML Bottle Box
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INGREDIENTS AND APPEARANCE
MD SCIENCE CANNABIDIOL
lidocaine and histamine dihydrochloride creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73615-103 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Lidocaine (UNII: 98PI200987) (Lidocaine - UNII:98PI200987) Lidocaine 37.8 mg in 1 mL Histamine Dihydrochloride (UNII: 3POA0Q644U) (Histamine - UNII:820484N8I3) Histamine Dihydrochloride 0.041 mg in 1 mL Inactive Ingredients Ingredient Name Strength Aloe Vera Leaf (UNII: ZY81Z83H0X) Caprylhydroxamic Acid (UNII: UPY805K99W) Caprylyl Glycol (UNII: 00YIU5438U) Carbomer Homopolymer Type C (Allyl Pentaerythritol Crosslinked) (UNII: 4Q93RCW27E) Cannabidiol (UNII: 19GBJ60SN5) Cetyl Esters Wax (UNII: D072FFP9GU) Coconut Oil (UNII: Q9L0O73W7L) Emu Oil (UNII: 344821WD61) Glycerin (UNII: PDC6A3C0OX) Glyceryl Monostearate (UNII: 230OU9XXE4) Isopropyl Palmitate (UNII: 8CRQ2TH63M) Dimethyl Sulfone (UNII: 9H4PO4Z4FT) Sodium Hydroxide (UNII: 55X04QC32I) Sorbitol (UNII: 506T60A25R) Steareth-21 (UNII: 53J3F32P58) Stearyl Alcohol (UNII: 2KR89I4H1Y) Product Characteristics Color PINK Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73615-103-03 1 in 1 BOX 02/15/2020 1 88 mL in 1 BOTTLE, PLASTIC; 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 02/15/2020 Labeler - MD NATURAL HEALTH LLC (080706676) Establishment Name Address ID/FEI Business Operations PACKAGE SOLUTIONS LLC 054705875 MANUFACTURE(73615-103)