Label: CBD CLINIC DEEP-RUB PAIN RELIEF - LEVEL 1- camphor oil
-
Contains inactivated NDC Code(s)
NDC Code(s): 24909-752-12, 24909-752-28, 24909-752-64 - Packager: Aidance Skincare & Topical Solutions, 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 December 29, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
-
Warnings
For external use only
Do not use on
• wounds or damaged skin
When using this product
• avoid contact with eyes or mucous membranes
• do not bandage tightly or use with a heating pad
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 skin irritation develops
If pregnant or breast-feeding
ask a health professional before use
Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center immediately - Directions
- Inactive Ingredients
- Questions?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
CBD CLINIC DEEP-RUB PAIN RELIEF - LEVEL 1
camphor oilProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:24909-752 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL) 3 g in 100 mL Inactive Ingredients Ingredient Name Strength CLOVE OIL (UNII: 578389D6D0) COTTONSEED OIL (UNII: H3E878020N) EUCALYPTUS OIL (UNII: 2R04ONI662) HEMP (UNII: TD1MUT01Q7) JOJOBA OIL (UNII: 724GKU717M) TEA TREE OIL (UNII: VIF565UC2G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:24909-752-12 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/15/2019 2 NDC:24909-752-28 3785 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/15/2019 3 NDC:24909-752-64 1893 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/15/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 10/15/2019 Labeler - Aidance Skincare & Topical Solutions, LLC (018950611) Establishment Name Address ID/FEI Business Operations Aidance Skincare & Topical Solutions, LLC 018950611 manufacture(24909-752) , label(24909-752)
