Label: HEMPNESIC- menthol, camphor gel
- NDC Code(s): 63347-223-01
- Packager: Blaine Labs Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 21, 2023
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- Official Label (Printer Friendly)
- DRUG FACTSActive Ingredients:
- Purpose
- Uses
- Warnings:
- Flammable:
- Ask a doctor before use if you have:
- When using this product:
- Stop use and contact your physician if:
- If pregnant or breast-feeding:
- Children under 2 years of age:
- Keep Out Of Reach Of Children:
- Directions:
- Other Information:
-
Inactive Ingredients
Ethyl Alcohol Denatured, D.I. Water, Glycerin, Propylene Glycol,
Cannabis Sativa Seed Oil (Hemp Seed Oil), Cannabidiol (CBD), Arnica Montana Flower
Extract (Arnica Oil), Mentha Piperita (Peppermint) Oil, Hydroxyethylcellulose, Carbomer,
triethanolamine, Mentha Viridis (Spearmint) Leaf Oil, Camellia Sinensis Leaf
Extract, Aloe Barbadensis Leaf Extract, Hamamelis Virginiana (Witch Hazel)
Extract, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Capsicum Annuum Fruit
Extract, Phenoxyethanol, Caprylyl Alcohol, Ethylhexyl Glycerin, Hexylene Glycol -
HempNesic®
PAIN-RELIEVING GEL
NDC 63347-223-01
BLAINE LABS®
HempNesic ®
PAIN-RELIEVING GELMENTHOL AND CAMPHOR
IN A GEL CONTAINING
CAPSAICIN & HEMP OIL3.0 OZ (88.7 mL)
DRUG FACTSActive Ingredients Purpose
Menthol 3.5% ................................Topical Analgesic
Camphor 0.2% ..............................Topical AnalgesicUses: For temporary relief from minor aches and
pains of sore muscles and joints asociated with:
• arthritis pain • backache • strains • sprainsWarnings: For external use only.
Flammable: Keep away from excessive heat or open flame.
Ask a doctor before use if you have: Sensitive skin
When using this product: • Avoid contact with the
eyes and/or mucous membranes • Do not use with
other sprays, ointments, creams or liniments • Do not
apply to irritated skin, & discontinue use if excessive
skin irritation develops • Do not bandage • Do not use
with heating pads or deviceStop use and contact your physician if: conditions
worsen, or if symptoms persist for more than seven (7)
days, or clear up and reoccur.If pregnant or breast-feeding: Ask a health
professional before useChildren under 2 years of age: Consult physician
Keep Out Of Reach Of Children: If swallowed, get
medical help or contact a poison control center immediately.Directions: Use only as directed. Rub a thin film
over the affected areas not more than four (4) times
daily. Rinse hands after use with cool water.Other Information: Store in a cool, dry place with lid closed tightly.
Inactive Ingredients: Ethyl Alcohol Denatured, D.I. Water,
Glycerin, Propylene Glycol, Cannabis Sativa Seed Oil (Hemp Seed Oil ),
Cannabidiol (Cbd), Arnica Montana Flower Extract (Arnica Oil),
Mentha Piperita (Peppermint) Oil, Hydroxyethylcellulose, Carbomer,
Triethanolamine, Mentha Viridis (Spearmint) Leaf Oil, Camellia
Sinensis Leaf Extract, Aloe Barbadensis Leaf Extract,
Hamamelis Virginiana (Witch Hazel) Extract, Melaleuca Alternifolia (Tea Tree)
Leaf Oil, Capsicum Annuum Fruit Extract, Phenoxyethanol,
Caprylyl Alcohol, Ethylhexyl Glycerin, Hexylene Glycol
Manufactured By: Blaine Labs, Inc. 11037 Lockport Place, Santa Fe Springs, CA 90670
Questions or Comments? Call (800) 307-8818 M-F 8am - 5pm (PST) *MADE IN THE USAHempnesic_223_01.jpg
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INGREDIENTS AND APPEARANCE
HEMPNESIC
menthol, camphor gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63347-223 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 3.5 g in 100 mL CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) .2 g in 100 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) Water (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S) CANNABIDIOL (UNII: 19GBJ60SN5) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) PEPPERMINT OIL (UNII: AV092KU4JH) CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT) CARBOMER 1342 (UNII: 809Y72KV36) TROLAMINE (UNII: 9O3K93S3TK) SPEARMINT OIL (UNII: C3M81465G5) GREEN TEA LEAF (UNII: W2ZU1RY8B0) ALOE VERA LEAF (UNII: ZY81Z83H0X) HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY) TEA TREE OIL (UNII: VIF565UC2G) PAPRIKA (UNII: X72Z47861V) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLIC ALCOHOL (UNII: NV1779205D) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) HEXYLENE GLYCOL (UNII: KEH0A3F75J) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63347-223-01 88.7 mL in 1 TUBE; Type 0: Not a Combination Product 04/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 04/01/2018 Labeler - Blaine Labs Inc. (017314571) Establishment Name Address ID/FEI Business Operations Blaine Labs Inc. 017314571 manufacture(63347-223)