SPA/POOL DETOX 6027- spa/pool detox liquid

Spa/Pool Detox by

Drug Labeling and Warnings

Spa/Pool Detox by is a Homeopathic medication manufactured, distributed, or labeled by Professional Complementary Health Formulas, Natural Pharmaceutical Manufacturing LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Sodium carbonate 12X
Pool water 12X, 30X, 60X
Spa water 12X, 30X, 60X
Algaecide 30X
Brominating tablets 30X
Bromium 30X
Clarifier 30X
Chlorinum 30X
Spa oxidizer 30X
Spa stain/scale 30X
Sodium bisulfate 30X
Cryptosporidium 30X, 60X, 100X
Escherichia coli 30X, 60X, 100X

QUESTIONS

Professional Formulas

PO Box 2034 Lake Oswego, OR 97035

INDICATIONS

For the temporary relief of skin irritations, red or watery eyes, minor earache, stomach cramps, diarrhea, or vomiting due to sensitivity to or exposure to pool or spa chemicals or contaminants.*

PURPOSE

*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS

Consult a doctor if condition worsens or symptoms persist. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use.

Keep out of the reach of children.

If pregnant or breastfeeding, ask a healthcare professional before use.

DIRECTIONS

Place drops under tongue 30 minutes before/after meals. Adults and children 12 years and over: Take 10 drops up to 3 times per day. Consult a physician for use in children under 12 years of age.

OTHER INFORMATION

Tamper resistant. If seal is broken, do not use. After opening, close container tightly and store at room temperature away from heat.

INACTIVE INGREDIENTS

20% ethanol, purified water.

LABEL

Est 1985

Professional Formulas

Complementary Health

Spa/Pool Detox

Homeopathic Remedy

2 FL. OZ. (59 mL)

INGREDIENTS AND APPEARANCE

SPA/POOL DETOX  6027
spa/pool detox liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63083-6027
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CARBONATE (UNII: 45P3261C7T) (CARBONATE ION - UNII:7UJQ5OPE7D)	SODIUM CARBONATE	12 [hp_X]  in 59 mL
CHLORINE (UNII: 4R7X1O2820) (CHLORINE - UNII:4R7X1O2820)	CHLORINE	12 [hp_X]  in 59 mL
CUPRIC CATION (UNII: 8CBV67279L) (CUPRIC CATION - UNII:8CBV67279L)	CUPRIC CATION	30 [hp_X]  in 59 mL
BROMINE (UNII: SBV4XY874G) (BROMINE - UNII:SBV4XY874G)	BROMINE	30 [hp_X]  in 59 mL
AMMONIUM CATION (UNII: 54S68520I4) (AMMONIUM CATION - UNII:54S68520I4)	AMMONIUM CATION	30 [hp_X]  in 59 mL
SODIUM CATION (UNII: LYR4M0NH37) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CATION	30 [hp_X]  in 59 mL
ETIDRONIC ACID (UNII: M2F465ROXU) (ETIDRONIC ACID - UNII:M2F465ROXU)	ETIDRONIC ACID	30 [hp_X]  in 59 mL
CRYPTOSPORIDIUM HOMINIS (UNII: DKE8M34J72) (CRYPTOSPORIDIUM HOMINIS - UNII:DKE8M34J72)	CRYPTOSPORIDIUM HOMINIS	30 [hp_X]  in 59 mL
ESCHERICHIA COLI (UNII: 514B9K0L10) (ESCHERICHIA COLI - UNII:514B9K0L10)	ESCHERICHIA COLI	30 [hp_X]  in 59 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63083-6027-2	59 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	08/15/1985

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		08/15/1984

Labeler - Professional Complementary Health Formulas (167339027)

Registrant - Natural Pharmaceutical Manufacturing LLC (015624923)

Establishment
Name	Address	ID/FEI	Business Operations
Natural Pharmaceutical Manufacturing LLC		015624923	manufacture(63083-6027)