OTC Medication Information: ORCHID BY H E B ANTIBACTERIAL MOISTURIZING VANILLA AND APPLE BLOSSOM

ORCHID BY H E B ANTIBACTERIAL MOISTURIZING VANILLA AND APPLE BLOSSOM- triclosan liquid
H E B

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.

ACTIVE INGREDIENT

TRICLOSAN 0.3%

PURPOSE

ANTIBACTERIAL

USES

TO HELP REDUCE BACTERIA ON THE SKIN

WARNINGS

FOR EXTERNAL USE ONLY

WHEN USING THIS PRODUCT

AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE WITH WATER

STOP USING THIS PRODUCT AND ASK DOCTOR IF

IRRITATION OR REDNESS DEVELOPS AND LASTS

KEEP OUT OF REACH OF CHILDREN

IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY

DIRECTIONS

APPLY TO WET HANDS, LATHER AND RINSE THOROUGHLY

QUESTIONS/COMMENTS?

1-866-695-3030

INACTIVE INGREDIENTS

WATER (AQUA), SODIUM LAURETH SULFATE, ACRYLATES COPOLYMER, GLYCOL DISTEARATE, COCAMIDOPROPYL BETAINE, MYRISTYL ALCOHOL, GLYCERIN, AMMONIUM CHLORIDE, GLYCERETH-26, COCO-GLUCOSIDE, GLYCERYL OLEATE, LAURYL LACTYL LACTATE, VANILL PLANIFOLIA FRUIT EXTRACT, PYRUS MALUS (APPLE) FRUIT EXTRACT, TOCOPHERYL ACETATE, BENZOPHENONE-4, DISODIUM EDTA, SODIUM HYDROXIDE, CITRIC ACID, BENZYL ALCOHOL, FRAGRANCE (PARFUM), MANNITOL, CELLULOSE, HYDROYXPROPYL METHYLCELLULOSE, RETINYL PALMITATE, IRON OXIDES (CI 77491), RED 33 (CI 17200), MICA (CI 77019), TITANIUM DIOXIDE (CI 77891), METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE

LABEL COPY

IMAGE OF THE LABEL
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ORCHID BY H E B ANTIBACTERIAL MOISTURIZING VANILLA AND APPLE BLOSSOM
triclosan liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-071
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICLOSAN (TRICLOSAN) TRICLOSAN 3 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER
SODIUM LAURETH SULFATE
METHACRYLIC ACID — METHYL METHACRYLATE COPOLYMER (1:1)
GLYCOL DISTEARATE
COCAMIDOPROPYL BETAINE
MYRISTYL ALCOHOL
GLYCERIN
AMMONIUM CHLORIDE
GLYCERETH-26
COCO GLUCOSIDE
GLYCERYL OLEATE
LAURYL LACTATE
VANILLA
APPLE
.ALPHA.-TOCOPHEROL ACETATE
SULISOBENZONE
EDETATE DISODIUM
SODIUM HYDROXIDE
CITRIC ACID MONOHYDRATE
BENZYL ALCOHOL
MANNITOL
POWDERED CELLULOSE
HYPROMELLOSES
VITAMIN A PALMITATE
FERRIC OXIDE RED
D&C RED NO. 33
MICA
TITANIUM DIOXIDE
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:37808-071-08 236 mL in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 01/18/2015
Labeler — H E B (007924756)
Registrant — APOLLO HEALTH AND BEAUTY CARE (201901209)
Establishment
Name Address ID/FEI Operations
APOLLO HEALTH AND BEAUTY CARE 201901209 manufacture (37808-071)

Revised: 01/2015 H E B

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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