Label: WELL AT WALGREENS ANTI-ITCH MAXIMUM STRENGTH- benzocaine and resorcinol cream
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Contains inactivated NDC Code(s)
NDC Code(s): 47046-181-01 - Packager: Anicare Pharmaceuticals Pvt. Ltd
- Category: HUMAN OTC DRUG LABEL
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 20, 2020
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Use
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Warnings
For external use only
- Directions
- Other information
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Inactive ingredients
aloe vera gel, carbomer, cetyl alcohol, corn oil, disodium EDTA, fragrance, glyceryl stearate, isopropyl myristate, isopropyl palmitate, lanolin, methyl-4 hydroxybenzoate, mineral oil, PEG-100 stearate, propylene glycol, purified water, stearic acid, stearyl alcohol, triethanolamine, vitamin A, E & D
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Principal display panel - 28 g Carton Label
Well at Walgreens
WALGREENS PHARMACIST RECOMMENDED‡
NEW
MAXIMUM STRENGTH
Anti-Itch Cream
Pain Relieving Cream
- Instantly soothes & relieves external itching & burning
- Soothes irritated skin with aloe
- Helps prevent further irritation
- Fresh, clean scent
Compared to Vaglsil® Maximum Strength active ingredients‡‡
Relieves vaginal itching.
NDC 0363-0674-64
Well at Walgreens
WALGREENS PHARMACIST RECOMMENDED‡
MAXIMUM STRENGTH
Anti-Itch Cream
Pain Relieving Cream
NET WT 1 OZ (28 g)
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INGREDIENTS AND APPEARANCE
WELL AT WALGREENS ANTI-ITCH MAXIMUM STRENGTH
benzocaine and resorcinol creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47046-181 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 20 g in 100 g RESORCINOL (UNII: YUL4LO94HK) (RESORCINOL - UNII:YUL4LO94HK) RESORCINOL 3 g in 100 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) CETYL ALCOHOL (UNII: 936JST6JCN) CORN OIL (UNII: 8470G57WFM) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) LANOLIN (UNII: 7EV65EAW6H) METHYLPARABEN (UNII: A2I8C7HI9T) MINERAL OIL (UNII: T5L8T28FGP) PEG-100 STEARATE (UNII: YD01N1999R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) STEARIC ACID (UNII: 4ELV7Z65AP) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) TROLAMINE (UNII: 9O3K93S3TK) VITAMIN A (UNII: 81G40H8B0T) VITAMIN D (UNII: 9VU1KI44GP) .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47046-181-01 28 g in 1 TUBE; Type 0: Not a Combination Product 07/27/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part346 07/27/2016 Labeler - Anicare Pharmaceuticals Pvt. Ltd (916837425)