BATH BOMB 2-PACK (ROSE)- allantoin tablet, soluble BATH BOMB 2-PACK (LAVENDER)- allantoin tablet, soluble BATH BOMB 2-PACK (ORANGE)- allantoin tablet, soluble BATH BOMB 2-PACK (LEMON)- allantoin tablet, soluble BATH BOMB 6-PACK (LAVENDER)- allantoin tablet, soluble BATH BOMB 2-PACK (EUCALYPTUS)- allantoin tablet, soluble BATH BOMB 6-PACK (ORANGE)- allantoin tablet, soluble BATH BOMB 6-PACK (ROSE)- allantoin tablet, soluble BATH BOMB 6-PACK (PEPPERMINT)- allantoin tablet, soluble BATH BOMB 6-PACK (LEMON)- allantoin tablet, soluble BATH BOMB 2-PACK (PEPPERMINT)- allantoin tablet, soluble BATH BOMB 6-PACK (EUCALYPTUS)- allantoin tablet, soluble

Bath Bomb 6-pack (Eucalyptus) by

Drug Labeling and Warnings

Bath Bomb 6-pack (Eucalyptus) by is a Otc medication manufactured, distributed, or labeled by Carolina Cannabis Creations LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Allantoin 0.5%

Sodium Bicarbonate 40%

Purpose

Skin Protectant

Skin Protectant

uses

Temporarily protects minor cuts, burns, scrapes, chafed, chapped, or cracked skin.

Warnings

For external use only.

Keep out of reach of children

Keep out of reach of children

When using this product

Do not get into eyes

Stop use and ask a doctor if

The condition worsens, symptoms last more than 7 days or clear up and occur again within a few days

Stop use and ask a doctor if

Condition worsens, symptoms last more than 7 days or clears up and occurs again within a few days

Do not use on

Deep or puncture wounds, animal bites, serious burns.

if pregnant or breast feeding

consult a health professional before use.

in case of overdose

seek medical help or contact a poison control center right away.

Directions

Adults and children 2 years and over. For use as soak in bath, dissolve 1 bath bomb in warm tub of water, Soak for 10 to 30 minutes as needed, or as directed by doctor. Pat dry (do not rub) to leave a thin layer on the skin

other information

store at 20-25C (68-77 F)

Inactive ingredients

Cannabidiol (CBD) Isolate, Citric acid, Corn Starch, essential oils, Jojoba oil, Magnesium Sulfate (Epsom salts), Mica powder, polysorbate 80.

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back label

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INGREDIENTS AND APPEARANCE

BATH BOMB 2-PACK (ROSE) 
allantoin tablet, soluble

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82876-504
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	1.1 g  in 186.16 g
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20)	SODIUM BICARBONATE	82 g  in 186.16 g

Inactive Ingredients
Ingredient Name	Strength
POLYSORBATE 80 (UNII: 6OZP39ZG8H)	1.9 g  in 186.16 g
STARCH, CORN (UNII: O8232NY3SJ)	18.7 g  in 186.16 g
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)	38 g  in 186.16 g
MICA (UNII: V8A1AW0880)	0.7 g  in 186.16 g
JOJOBA OIL (UNII: 724GKU717M)	2.7 g  in 186.16 g
CANNABIDIOL (UNII: 19GBJ60SN5)	0.21 g  in 186.16 g
ROSE OIL (UNII: WUB68Y35M7)	3.25 g  in 186.16 g
MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)	37.6 g  in 186.16 g

Product Characteristics
Color	pink	Score	score with uneven pieces
Shape	ROUND	Size	55mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82876-504-02	186.16 g in 1 BOX; Type 0: Not a Combination Product	08/06/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	08/06/2025

BATH BOMB 2-PACK (LAVENDER) 
allantoin tablet, soluble

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82876-502
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	1.1 g  in 186.16 g
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20)	SODIUM BICARBONATE	82 g  in 186.16 g

Inactive Ingredients
Ingredient Name	Strength
POLYSORBATE 80 (UNII: 6OZP39ZG8H)	1.9 g  in 186.16 g
STARCH, CORN (UNII: O8232NY3SJ)	18.7 g  in 186.16 g
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)	38 g  in 186.16 g
MICA (UNII: V8A1AW0880)	0.7 g  in 186.16 g
JOJOBA OIL (UNII: 724GKU717M)	2.7 g  in 186.16 g
CANNABIDIOL (UNII: 19GBJ60SN5)	0.21 g  in 186.16 g
LAVENDER OIL (UNII: ZBP1YXW0H8)	3.25 g  in 186.16 g
MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)	37.6 g  in 186.16 g

Product Characteristics
Color	purple	Score	score with uneven pieces
Shape	ROUND	Size	55mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82876-502-02	186.16 g in 1 BOX; Type 0: Not a Combination Product	08/06/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	08/06/2025

BATH BOMB 2-PACK (ORANGE) 
allantoin tablet, soluble

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82876-503
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	1.1 g  in 187.91 g
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20)	SODIUM BICARBONATE	82 g  in 187.91 g

Inactive Ingredients
Ingredient Name	Strength
POLYSORBATE 80 (UNII: 6OZP39ZG8H)	1.9 g  in 187.91 g
STARCH, CORN (UNII: O8232NY3SJ)	18.7 g  in 187.91 g
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)	38 g  in 187.91 g
MICA (UNII: V8A1AW0880)	0.7 g  in 187.91 g
JOJOBA OIL (UNII: 724GKU717M)	2.7 g  in 187.91 g
CANNABIDIOL (UNII: 19GBJ60SN5)	0.21 g  in 187.91 g
MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)	37.6 g  in 187.91 g
ORANGE OIL (UNII: AKN3KSD11B)	5 g  in 187.91 g

Product Characteristics
Color	orange	Score	score with uneven pieces
Shape	ROUND	Size	55mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82876-503-02	187.91 g in 1 BOX; Type 0: Not a Combination Product	08/06/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	08/06/2025

BATH BOMB 2-PACK (LEMON) 
allantoin tablet, soluble

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82876-501
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	1.1 g  in 187.91 g
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20)	SODIUM BICARBONATE	82 g  in 187.91 g

Inactive Ingredients
Ingredient Name	Strength
POLYSORBATE 80 (UNII: 6OZP39ZG8H)	1.9 g  in 187.91 g
STARCH, CORN (UNII: O8232NY3SJ)	18.7 g  in 187.91 g
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)	38 g  in 187.91 g
MICA (UNII: V8A1AW0880)	0.7 g  in 187.91 g
JOJOBA OIL (UNII: 724GKU717M)	2.7 g  in 187.91 g
CANNABIDIOL (UNII: 19GBJ60SN5)	0.21 g  in 187.91 g
LEMON OIL (UNII: I9GRO824LL)	5 g  in 187.91 g
MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)	37.6 g  in 187.91 g

Product Characteristics
Color	yellow	Score	score with uneven pieces
Shape	ROUND	Size	55mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82876-501-02	187.91 g in 1 BOX; Type 0: Not a Combination Product	08/06/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	08/06/2025

BATH BOMB 6-PACK (LAVENDER) 
allantoin tablet, soluble

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82876-508
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	3.1 g  in 555.3 g
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20)	SODIUM BICARBONATE	248 g  in 555.3 g

Inactive Ingredients
Ingredient Name	Strength
POLYSORBATE 80 (UNII: 6OZP39ZG8H)	5.7 g  in 555.3 g
STARCH, CORN (UNII: O8232NY3SJ)	56 g  in 555.3 g
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)	112 g  in 555.3 g
MICA (UNII: V8A1AW0880)	2.1 g  in 555.3 g
JOJOBA OIL (UNII: 724GKU717M)	8 g  in 555.3 g
CANNABIDIOL (UNII: 19GBJ60SN5)	0.65 g  in 555.3 g
LAVENDER OIL (UNII: ZBP1YXW0H8)	9.75 g  in 555.3 g
MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)	113 g  in 555.3 g

Product Characteristics
Color	purple	Score	score with uneven pieces
Shape	ROUND	Size	55mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82876-508-06	555.3 g in 1 BOX; Type 0: Not a Combination Product	08/06/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	08/06/2025

BATH BOMB 2-PACK (EUCALYPTUS) 
allantoin tablet, soluble

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82876-506
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	1.1 g  in 186.16 g
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20)	SODIUM BICARBONATE	82 g  in 186.16 g

Inactive Ingredients
Ingredient Name	Strength
POLYSORBATE 80 (UNII: 6OZP39ZG8H)	1.9 g  in 186.16 g
STARCH, CORN (UNII: O8232NY3SJ)	18.7 g  in 186.16 g
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)	38 g  in 186.16 g
MICA (UNII: V8A1AW0880)	0.7 g  in 186.16 g
JOJOBA OIL (UNII: 724GKU717M)	2.7 g  in 186.16 g
CANNABIDIOL (UNII: 19GBJ60SN5)	0.21 g  in 186.16 g
EUCALYPTUS OIL (UNII: 2R04ONI662)	3.25 g  in 186.16 g
MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)	37.6 g  in 186.16 g

Product Characteristics
Color	white	Score	score with uneven pieces
Shape	ROUND	Size	55mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82876-506-02	186.16 g in 1 BOX; Type 0: Not a Combination Product	08/06/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	08/06/2025

BATH BOMB 6-PACK (ORANGE) 
allantoin tablet, soluble

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82876-509
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	3.1 g  in 560.55 g
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20)	SODIUM BICARBONATE	248 g  in 560.55 g

Inactive Ingredients
Ingredient Name	Strength
POLYSORBATE 80 (UNII: 6OZP39ZG8H)	5.7 g  in 560.55 g
STARCH, CORN (UNII: O8232NY3SJ)	56 g  in 560.55 g
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)	112 g  in 560.55 g
MICA (UNII: V8A1AW0880)	2.1 g  in 560.55 g
JOJOBA OIL (UNII: 724GKU717M)	8 g  in 560.55 g
CANNABIDIOL (UNII: 19GBJ60SN5)	0.65 g  in 560.55 g
ORANGE OIL (UNII: AKN3KSD11B)	15 g  in 560.55 g
MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)	113 g  in 560.55 g

Product Characteristics
Color	orange	Score	score with uneven pieces
Shape	ROUND	Size	55mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82876-509-06	206.01 g in 1 BOX; Type 0: Not a Combination Product	08/06/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	08/06/2025

BATH BOMB 6-PACK (ROSE) 
allantoin tablet, soluble

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82876-510
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	3.1 g  in 555.3 g
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20)	SODIUM BICARBONATE	248 g  in 555.3 g

Inactive Ingredients
Ingredient Name	Strength
POLYSORBATE 80 (UNII: 6OZP39ZG8H)	5.7 g  in 555.3 g
STARCH, CORN (UNII: O8232NY3SJ)	56 g  in 555.3 g
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)	112 g  in 555.3 g
MICA (UNII: V8A1AW0880)	2.1 g  in 555.3 g
JOJOBA OIL (UNII: 724GKU717M)	8 g  in 555.3 g
CANNABIDIOL (UNII: 19GBJ60SN5)	0.65 g  in 555.3 g
ROSE OIL (UNII: WUB68Y35M7)	9.75 g  in 555.3 g
MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)	113 g  in 555.3 g

Product Characteristics
Color	pink	Score	score with uneven pieces
Shape	ROUND	Size	55mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82876-510-06	555.3 g in 1 BOX; Type 0: Not a Combination Product	08/06/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	08/06/2025

BATH BOMB 6-PACK (PEPPERMINT) 
allantoin tablet, soluble

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82876-511
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	3.1 g  in 555.3 g
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20)	SODIUM BICARBONATE	248 g  in 555.3 g

Inactive Ingredients
Ingredient Name	Strength
POLYSORBATE 80 (UNII: 6OZP39ZG8H)	5.7 g  in 555.3 g
STARCH, CORN (UNII: O8232NY3SJ)	56 g  in 555.3 g
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)	112 g  in 555.3 g
MICA (UNII: V8A1AW0880)	2.1 g  in 555.3 g
JOJOBA OIL (UNII: 724GKU717M)	8 g  in 555.3 g
CANNABIDIOL (UNII: 19GBJ60SN5)	0.65 g  in 555.3 g
PEPPERMINT OIL (UNII: AV092KU4JH)	9.75 g  in 555.3 g
MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)	113 g  in 555.3 g

Product Characteristics
Color	black	Score	score with uneven pieces
Shape	ROUND	Size	55mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82876-511-06	555.3 g in 1 BOX; Type 0: Not a Combination Product	08/06/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	08/06/2025

BATH BOMB 6-PACK (LEMON) 
allantoin tablet, soluble

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82876-507
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	3.1 g  in 560.55 g
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20)	SODIUM BICARBONATE	248 g  in 560.55 g

Inactive Ingredients
Ingredient Name	Strength
POLYSORBATE 80 (UNII: 6OZP39ZG8H)	5.7 g  in 560.55 g
STARCH, CORN (UNII: O8232NY3SJ)	56 g  in 560.55 g
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)	112 g  in 560.55 g
MICA (UNII: V8A1AW0880)	2.1 g  in 560.55 g
JOJOBA OIL (UNII: 724GKU717M)	8 g  in 560.55 g
CANNABIDIOL (UNII: 19GBJ60SN5)	0.65 g  in 560.55 g
LEMON OIL (UNII: I9GRO824LL)	15 g  in 560.55 g
MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)	113 g  in 560.55 g

Product Characteristics
Color	yellow	Score	score with uneven pieces
Shape	ROUND	Size	55mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82876-507-06	206.01 g in 1 BOX; Type 0: Not a Combination Product	08/06/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	08/06/2025

BATH BOMB 2-PACK (PEPPERMINT) 
allantoin tablet, soluble

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82876-505
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	1.1 g  in 186.16 g
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20)	SODIUM BICARBONATE	82 g  in 186.16 g

Inactive Ingredients
Ingredient Name	Strength
POLYSORBATE 80 (UNII: 6OZP39ZG8H)	1.9 g  in 186.16 g
STARCH, CORN (UNII: O8232NY3SJ)	18.7 g  in 186.16 g
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)	38 g  in 186.16 g
MICA (UNII: V8A1AW0880)	0.7 g  in 186.16 g
JOJOBA OIL (UNII: 724GKU717M)	2.7 g  in 186.16 g
CANNABIDIOL (UNII: 19GBJ60SN5)	0.21 g  in 186.16 g
PEPPERMINT OIL (UNII: AV092KU4JH)	3.25 g  in 186.16 g
MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)	37.6 g  in 186.16 g

Product Characteristics
Color	black	Score	score with uneven pieces
Shape	ROUND	Size	55mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82876-505-02	186.16 g in 1 BOX; Type 0: Not a Combination Product	08/06/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	08/06/2025

BATH BOMB 6-PACK (EUCALYPTUS) 
allantoin tablet, soluble

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82876-512
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	3.1 g  in 555.3 g
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20)	SODIUM BICARBONATE	248 g  in 555.3 g

Inactive Ingredients
Ingredient Name	Strength
POLYSORBATE 80 (UNII: 6OZP39ZG8H)	5.7 g  in 555.3 g
STARCH, CORN (UNII: O8232NY3SJ)	56 g  in 555.3 g
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)	112 g  in 555.3 g
MICA (UNII: V8A1AW0880)	2.1 g  in 555.3 g
JOJOBA OIL (UNII: 724GKU717M)	8 g  in 555.3 g
CANNABIDIOL (UNII: 19GBJ60SN5)	0.65 g  in 555.3 g
EUCALYPTUS OIL (UNII: 2R04ONI662)	9.75 g  in 555.3 g
MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)	113 g  in 555.3 g

Product Characteristics
Color	black	Score	score with uneven pieces
Shape	ROUND	Size	55mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82876-512-06	555.3 g in 1 BOX; Type 0: Not a Combination Product	08/06/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	08/06/2025

Labeler - Carolina Cannabis Creations LLC (118697474)

Establishment
Name	Address	ID/FEI	Business Operations
Carolina Cannabis Creations LLC		118697474	manufacture(82876-502, 82876-501, 82876-503, 82876-504, 82876-505, 82876-506, 82876-507, 82876-508, 82876-509, 82876-510, 82876-511, 82876-512)